US6271195B1 - Aminimide-containing molecules and materials as molecular recognition agents - Google Patents
Aminimide-containing molecules and materials as molecular recognition agents Download PDFInfo
- Publication number
- US6271195B1 US6271195B1 US09/426,547 US42654799A US6271195B1 US 6271195 B1 US6271195 B1 US 6271195B1 US 42654799 A US42654799 A US 42654799A US 6271195 B1 US6271195 B1 US 6271195B1
- Authority
- US
- United States
- Prior art keywords
- aminimide
- composition
- group
- derivative
- different
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 *[C@@]([H])(C(C)C)N(C)C(=O)C(C)C.*[C@]([H])(/[NH+]=C(\[O-])C(C)C)C(C)C.CC(C)/C([O-])=N/[N+](C)(C)C(C)C.CC(C)C(=O)[N-][N+](C)(C)C(C)C Chemical compound *[C@@]([H])(C(C)C)N(C)C(=O)C(C)C.*[C@]([H])(/[NH+]=C(\[O-])C(C)C)C(C)C.CC(C)/C([O-])=N/[N+](C)(C)C(C)C.CC(C)C(=O)[N-][N+](C)(C)C(C)C 0.000 description 40
- WPGWNUVQBHBTKS-UHFFFAOYSA-N CC(=O)[N-][N+](C)(C)C.CC([O-])=N[N+](C)(C)C Chemical compound CC(=O)[N-][N+](C)(C)C.CC([O-])=N[N+](C)(C)C WPGWNUVQBHBTKS-UHFFFAOYSA-N 0.000 description 2
- XWJSGGDQJNTBAO-UHFFFAOYSA-N C.C.C.C=CC(=O)OC.CCCCC.COC(=O)CCNCCC1=CNC2=C1C=C(O)C=C2.C[N+](C)(CO)NC(=O)CCNCCC1=CNC2=C1C=C(O)C=C2.NCCC1=CNC2=C1C=C(O)C=C2.[V]I Chemical compound C.C.C.C=CC(=O)OC.CCCCC.COC(=O)CCNCCC1=CNC2=C1C=C(O)C=C2.C[N+](C)(CO)NC(=O)CCNCCC1=CNC2=C1C=C(O)C=C2.NCCC1=CNC2=C1C=C(O)C=C2.[V]I XWJSGGDQJNTBAO-UHFFFAOYSA-N 0.000 description 1
- DONTWVPBIZIVOL-UHFFFAOYSA-N C.C.C.CC(=O)[N-][N+](C)(C)CC(=O)Cl.CC(=O)[N-][N+](C)(C)CC(=O)Cl.CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C.CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C.CN(C)N Chemical compound C.C.C.CC(=O)[N-][N+](C)(C)CC(=O)Cl.CC(=O)[N-][N+](C)(C)CC(=O)Cl.CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C.CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C.CN(C)N DONTWVPBIZIVOL-UHFFFAOYSA-N 0.000 description 1
- PPXDXKWACRMAPC-UHFFFAOYSA-N C.C.C.CC(=O)[N-][N+](C)(C)CC(C)O.CC1CO1.CN(C)N.CO.COC(C)=O Chemical compound C.C.C.CC(=O)[N-][N+](C)(C)CC(C)O.CC1CO1.CN(C)N.CO.COC(C)=O PPXDXKWACRMAPC-UHFFFAOYSA-N 0.000 description 1
- OVDAQNVHMNWLOS-UHFFFAOYSA-N C.C.CC(=O)[N-][N+](C)(C)C.COC(C)=O.C[N+](C)(C)N Chemical compound C.C.CC(=O)[N-][N+](C)(C)C.COC(C)=O.C[N+](C)(C)N OVDAQNVHMNWLOS-UHFFFAOYSA-N 0.000 description 1
- ZEGHZBLCPXLNEC-SCGDHKLHSA-N C.C.CC1CO1.CN(C)N.[H][C@@](NC(=O)C1=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1)(C(=O)[N-][N+](C)(C)CC(C)O)C(C)C.[H][C@](COOC)(NC(=O)C1=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1)C(C)C Chemical compound C.C.CC1CO1.CN(C)N.[H][C@@](NC(=O)C1=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1)(C(=O)[N-][N+](C)(C)CC(C)O)C(C)C.[H][C@](COOC)(NC(=O)C1=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1)C(C)C ZEGHZBLCPXLNEC-SCGDHKLHSA-N 0.000 description 1
- UJHMDPYSGGBXPV-VLPRVVBRSA-O C.C.CC[N@+](C)(N)CC(=O)[N-][N@@+](C)(CC)C1=CC=CC=C1.CC[N@+](C)([N-]C(=O)C[N@+](C)(N)CC)C1=CC=CC=C1.CN(C)N.C[N+](C)(NC(=O)CBr)C1=CC=CC=C1.[Br-].[Br-] Chemical compound C.C.CC[N@+](C)(N)CC(=O)[N-][N@@+](C)(CC)C1=CC=CC=C1.CC[N@+](C)([N-]C(=O)C[N@+](C)(N)CC)C1=CC=CC=C1.CN(C)N.C[N+](C)(NC(=O)CBr)C1=CC=CC=C1.[Br-].[Br-] UJHMDPYSGGBXPV-VLPRVVBRSA-O 0.000 description 1
- NAZHJDMXPMDMGR-IXIVHGECSA-N C.C.CN(C)N.[H][C@@](C)(O)[C@@]([H])(C)O.[H][C@@](O)(C[N+](C)(C)NC(=O)[C@@]([H])(O)[C@]([H])(O)C(=O)[N-][N+](C)(C)C(C)(C)C)[Y][C@@]([H])(O)CC(C)(C)C.[H][C@]1([Y][C@]2([H])CO2)CO1 Chemical compound C.C.CN(C)N.[H][C@@](C)(O)[C@@]([H])(C)O.[H][C@@](O)(C[N+](C)(C)NC(=O)[C@@]([H])(O)[C@]([H])(O)C(=O)[N-][N+](C)(C)C(C)(C)C)[Y][C@@]([H])(O)CC(C)(C)C.[H][C@]1([Y][C@]2([H])CO2)CO1 NAZHJDMXPMDMGR-IXIVHGECSA-N 0.000 description 1
- OMPDMLYTJUSSSQ-YPXBFLFMSA-N C.C/C(C#C(=O)=O)=N\NC(=O)C1=CC=CC=C1.CC(=O)C#C(=O)=O.NNC(=O)C1=CC=CC=C1.[H]N(NC(=O)C1=CC=CC=C1)[C@@]([H])(C)C#C(=O)=O Chemical compound C.C/C(C#C(=O)=O)=N\NC(=O)C1=CC=CC=C1.CC(=O)C#C(=O)=O.NNC(=O)C1=CC=CC=C1.[H]N(NC(=O)C1=CC=CC=C1)[C@@]([H])(C)C#C(=O)=O OMPDMLYTJUSSSQ-YPXBFLFMSA-N 0.000 description 1
- FLKOXDWRUYIQBD-UHFFFAOYSA-N C.C=CC(=O)NC(C)(C)C(=O)[N-][N+](C)(C)C1=CC=C(C=C)C=C1.C=CC1=CC=C([N+](C)(C)N)C=C1.C=CC1=NC(C)(C)C(=O)O1 Chemical compound C.C=CC(=O)NC(C)(C)C(=O)[N-][N+](C)(C)C1=CC=C(C=C)C=C1.C=CC1=CC=C([N+](C)(C)N)C=C1.C=CC1=NC(C)(C)C(=O)O1 FLKOXDWRUYIQBD-UHFFFAOYSA-N 0.000 description 1
- BRTCRMCTUXEJAH-ATTARECDSA-N C.C=CC1=NC(C)(C)C(=O)O1.CNC1=CC=C(NCCO[3H]=S)C2=C1C(=O)C1=C(C=CC=C1)C2=O.CNC1=CC=C(NCC[N+](C)(C)[N-]C(=O)C(C)(C)NC(=O)CCN2CCC34C5=C6/C=C(OC)/C=C\5CC2C3C=CC(O)C4O6)C2=C1C(=O)C1=C(C=CC=C1)C2=O.COC1=CC2=C3C(=C1)CC(NCCC1=NC(C)(C)C(=O)O1)C1C=CC(O)C(O2)C31.[H]N1CCC23C4=C5C=C(OC)C=C4CC1C2C=CC(O)C3O5 Chemical compound C.C=CC1=NC(C)(C)C(=O)O1.CNC1=CC=C(NCCO[3H]=S)C2=C1C(=O)C1=C(C=CC=C1)C2=O.CNC1=CC=C(NCC[N+](C)(C)[N-]C(=O)C(C)(C)NC(=O)CCN2CCC34C5=C6/C=C(OC)/C=C\5CC2C3C=CC(O)C4O6)C2=C1C(=O)C1=C(C=CC=C1)C2=O.COC1=CC2=C3C(=C1)CC(NCCC1=NC(C)(C)C(=O)O1)C1C=CC(O)C(O2)C31.[H]N1CCC23C4=C5C=C(OC)C=C4CC1C2C=CC(O)C3O5 BRTCRMCTUXEJAH-ATTARECDSA-N 0.000 description 1
- AMSVMNBIXWBWGN-UHFFFAOYSA-N C.CC(=O)Cl.CC(=O)NN(C)C.CN(C)N Chemical compound C.CC(=O)Cl.CC(=O)NN(C)C.CN(C)N AMSVMNBIXWBWGN-UHFFFAOYSA-N 0.000 description 1
- LWIZKCSSOIHAIE-UHFFFAOYSA-O C.CC(=O)NN1CCCCC1.CNC(=O)CBr.CNC(=O)C[N+]1(NC(C)=O)CCCCC1 Chemical compound C.CC(=O)NN1CCCCC1.CNC(=O)CBr.CNC(=O)C[N+]1(NC(C)=O)CCCCC1 LWIZKCSSOIHAIE-UHFFFAOYSA-O 0.000 description 1
- QGQONAUHUKIHMX-UHFFFAOYSA-N C.CC(=O)[N-][N+](C)(C)CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C.CC(=O)[N-][N+](C)(C)CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C Chemical compound C.CC(=O)[N-][N+](C)(C)CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C.CC(=O)[N-][N+](C)(C)CC(=O)[N-][N+](C)(C)CC(=O)NN(C)C QGQONAUHUKIHMX-UHFFFAOYSA-N 0.000 description 1
- RXTOSJRDKJJOPT-OBQQFSEGSA-N C.CC(C)(C)O[K].CC[C@@](CC1=CC=CC=C1)(NC(=O)CCSC)C(=O)[N-][N+](C)(CC)C1=CC=CC=C1.CC[C@@]1(CC2=CC=CC=C2)N=C(CCSC)OC1=O.CC[N+](C)(N)C1=CC=CC=C1.[I-] Chemical compound C.CC(C)(C)O[K].CC[C@@](CC1=CC=CC=C1)(NC(=O)CCSC)C(=O)[N-][N+](C)(CC)C1=CC=CC=C1.CC[C@@]1(CC2=CC=CC=C2)N=C(CCSC)OC1=O.CC[N+](C)(N)C1=CC=CC=C1.[I-] RXTOSJRDKJJOPT-OBQQFSEGSA-N 0.000 description 1
- PEPRXCDLNUFXGM-RIFJDKNASA-N C.CC(C)C1=CC=C(NC(=O)CCl)C=C1.CC(C)C1=CC=C(NC(=O)C[N@@+](C)(N)CC2=CC=CC=C2)C=C1.CN(N)CC1=CC=CC=C1.[I-].[K]I Chemical compound C.CC(C)C1=CC=C(NC(=O)CCl)C=C1.CC(C)C1=CC=C(NC(=O)C[N@@+](C)(N)CC2=CC=CC=C2)C=C1.CN(N)CC1=CC=CC=C1.[I-].[K]I PEPRXCDLNUFXGM-RIFJDKNASA-N 0.000 description 1
- PMOYVBRKCNEOSP-CQIXXRNHSA-O C.CC(C)C1=CC=C(NC(=O)C[N@+](C)(CC2=CNC(=O)N(C)C2=O)[N-]C(=O)CCl)C=C1.CC(C)C1=CC=C(NC(=O)C[N@@+](C)(N)CC2=CNC(=O)N(C)C2=O)C=C1.O=C(Cl)CCl.[I-] Chemical compound C.CC(C)C1=CC=C(NC(=O)C[N@+](C)(CC2=CNC(=O)N(C)C2=O)[N-]C(=O)CCl)C=C1.CC(C)C1=CC=C(NC(=O)C[N@@+](C)(N)CC2=CNC(=O)N(C)C2=O)C=C1.O=C(Cl)CCl.[I-] PMOYVBRKCNEOSP-CQIXXRNHSA-O 0.000 description 1
- WASXTZWZABHNDA-SUKKNWNLSA-O C.CC(C)C1=CC=C(NC(=O)C[N@+](C)(CC2=CNC(=O)N(C)C2=O)[N-]C(=O)CCl)C=C1.CC(C)CN(C)NC(=O)C(F)(F)F.CC(C)C[N@@+](C)(CC(=O)[N-][N@+](C)(CC(=O)NC1=CC=C(C(C)C)C=C1)CC1=CNC(=O)N(C)C1=O)NC(=O)C(F)(F)F Chemical compound C.CC(C)C1=CC=C(NC(=O)C[N@+](C)(CC2=CNC(=O)N(C)C2=O)[N-]C(=O)CCl)C=C1.CC(C)CN(C)NC(=O)C(F)(F)F.CC(C)C[N@@+](C)(CC(=O)[N-][N@+](C)(CC(=O)NC1=CC=C(C(C)C)C=C1)CC1=CNC(=O)N(C)C1=O)NC(=O)C(F)(F)F WASXTZWZABHNDA-SUKKNWNLSA-O 0.000 description 1
- UPPZURRHMOYUGV-TUXSZDOYSA-N C.CC(C)C1=CC=C(NC(=O)C[N@@+](C)(N)CC2=CNC(=O)N(C)C2=O)C=C1.CC(C)C1=CC=C(NC(=O)Cl)C=C1.CN(N)CC1=CNC(=O)N(C)C1=O.[I-].[K]I Chemical compound C.CC(C)C1=CC=C(NC(=O)C[N@@+](C)(N)CC2=CNC(=O)N(C)C2=O)C=C1.CC(C)C1=CC=C(NC(=O)Cl)C=C1.CN(N)CC1=CNC(=O)N(C)C1=O.[I-].[K]I UPPZURRHMOYUGV-TUXSZDOYSA-N 0.000 description 1
- MVLPXZCZYPPYSY-UHFFFAOYSA-N C.CC.CCN(CC)CCC(=O)[N-][N+](C)(C)CC(O)COCCC[Si](C)(C)O[Si](C)(C)C.CCNC.CN(C)N Chemical compound C.CC.CCN(CC)CCC(=O)[N-][N+](C)(C)CC(O)COCCC[Si](C)(C)O[Si](C)(C)C.CCNC.CN(C)N MVLPXZCZYPPYSY-UHFFFAOYSA-N 0.000 description 1
- KHZJBFFIGLVXNW-UHFFFAOYSA-N C.CC.CO.C[Si](C)(C)O.C[Si](C)(C)O[Si](C)(C)CCCOCC1CO1.O.O[SiH2]CCCOCC1CO1 Chemical compound C.CC.CO.C[Si](C)(C)O.C[Si](C)(C)O[Si](C)(C)CCCOCC1CO1.O.O[SiH2]CCCOCC1CO1 KHZJBFFIGLVXNW-UHFFFAOYSA-N 0.000 description 1
- ZJIFEOBOPDXKLN-QXMDUVAESA-N C.CC1=CC([N+](=O)[O-])=CC(C(=O)Cl)=C1.[H][C@@](N)(C(=O)OC)C(C)C.[H][C@@](NC(=O)C1=CC(C)=CC(C)=C1)(C(=O)OC)C(C)C Chemical compound C.CC1=CC([N+](=O)[O-])=CC(C(=O)Cl)=C1.[H][C@@](N)(C(=O)OC)C(C)C.[H][C@@](NC(=O)C1=CC(C)=CC(C)=C1)(C(=O)OC)C(C)C ZJIFEOBOPDXKLN-QXMDUVAESA-N 0.000 description 1
- AMJMCNZHPVUYOK-GUVJSQNXSA-P C.CC1=NC(C)(C)C(=O)O1.[H][C@](C)(NC(=O)[C@@]([H])(C)NC(=O)[C@@]([H])(C)NCC(=O)N[N+](C)(C)CN)C(C)=O.[H][C@](C)(NC(=O)[C@@]([H])(C)NC(=O)[C@@]([H])(C)NCC(=O)N[N+](C)(C)CNC(=O)C(C)(C)NC(C)=O)C(=O)O Chemical compound C.CC1=NC(C)(C)C(=O)O1.[H][C@](C)(NC(=O)[C@@]([H])(C)NC(=O)[C@@]([H])(C)NCC(=O)N[N+](C)(C)CN)C(C)=O.[H][C@](C)(NC(=O)[C@@]([H])(C)NC(=O)[C@@]([H])(C)NCC(=O)N[N+](C)(C)CNC(=O)C(C)(C)NC(C)=O)C(=O)O AMJMCNZHPVUYOK-GUVJSQNXSA-P 0.000 description 1
- RYEUOXDMZXEXCN-UHFFFAOYSA-N C.CCC12CCCN3CCC4C5=CC=CC=C5N(C4C31)C(O)(C(=O)OC)C2.CCCCCCCCCCC(O)CN(C)NC(=O)C1(O)CC2(CC)CCCN3CCC4C5=CC=CC=C5C1N4C32.CCCCCCCCCCC1CO1 Chemical compound C.CCC12CCCN3CCC4C5=CC=CC=C5N(C4C31)C(O)(C(=O)OC)C2.CCCCCCCCCCC(O)CN(C)NC(=O)C1(O)CC2(CC)CCCN3CCC4C5=CC=CC=C5C1N4C32.CCCCCCCCCCC1CO1 RYEUOXDMZXEXCN-UHFFFAOYSA-N 0.000 description 1
- HYYWWGIEQJUJGA-UHFFFAOYSA-N C.CCCCCOOCC.CCCl.O=C(O)CCCO Chemical compound C.CCCCCOOCC.CCCl.O=C(O)CCCO HYYWWGIEQJUJGA-UHFFFAOYSA-N 0.000 description 1
- HHPLWASORMROSE-OOBAUDMISA-O C.CC[N@+](C)(N)C1=CC=CC=C1.CC[N@+](C)(NC(=O)CBr)C1=CC=CC=C1.O=C(Cl)CBr.[I-] Chemical compound C.CC[N@+](C)(N)C1=CC=CC=C1.CC[N@+](C)(NC(=O)CBr)C1=CC=CC=C1.O=C(Cl)CBr.[I-] HHPLWASORMROSE-OOBAUDMISA-O 0.000 description 1
- QRTFYFAJYCLSRW-UHFFFAOYSA-N C.CN(C)C.CNC.NCl Chemical compound C.CN(C)C.CNC.NCl QRTFYFAJYCLSRW-UHFFFAOYSA-N 0.000 description 1
- SRAPDKKFLDEQQJ-UHFFFAOYSA-N C.CN(C)N.COC(=O)CCl.COC(=O)C[N+](C)(C)N.[Cl-] Chemical compound C.CN(C)N.COC(=O)CCl.COC(=O)C[N+](C)(C)N.[Cl-] SRAPDKKFLDEQQJ-UHFFFAOYSA-N 0.000 description 1
- ZLJBJYXOPFJOII-UHFFFAOYSA-N C.CNN1CCCCC1.NN1CCCCC1 Chemical compound C.CNN1CCCCC1.NN1CCCCC1 ZLJBJYXOPFJOII-UHFFFAOYSA-N 0.000 description 1
- UZHCLPOBVWZQDV-UHFFFAOYSA-N C.CO.COC(=O)C[N+](C)(C)N.C[N+](C)(N)CC(=O)[O-] Chemical compound C.CO.COC(=O)C[N+](C)(C)N.C[N+](C)(N)CC(=O)[O-] UZHCLPOBVWZQDV-UHFFFAOYSA-N 0.000 description 1
- SQJCZYPSWFRSRH-WSUZWAMDSA-O C.C[N+](C)(C)[N-]C(=O)CBr.[H][C@](C)(N)C(=O)N[C@]([H])(C)C(=O)N[C@]([H])(C)C(C)=O.[H][C@](C)(NC(=O)[C@@]([H])(C)NC(=O)[C@@]([H])(C)NCC(=O)N[N+](C)(C)C)C(C)=O Chemical compound C.C[N+](C)(C)[N-]C(=O)CBr.[H][C@](C)(N)C(=O)N[C@]([H])(C)C(=O)N[C@]([H])(C)C(C)=O.[H][C@](C)(NC(=O)[C@@]([H])(C)NC(=O)[C@@]([H])(C)NCC(=O)N[N+](C)(C)C)C(C)=O SQJCZYPSWFRSRH-WSUZWAMDSA-O 0.000 description 1
- NDCKPDXOQVCDRH-FHNHQRAVSA-N C.O.[H]C1C([H])(CO)OC([H])C([H])(N[Ac])C1([H])O.[H]C1OC(CO)[C@]([H])(O)C([H])(O)C1([H])[Y].[H]C1OC([H])(CO)[C@]([H])(O)C([H])(O)C1([H])OC1(C)OC([H])(C)[C@]([H])(O)C([H])(O)C1([H])O Chemical compound C.O.[H]C1C([H])(CO)OC([H])C([H])(N[Ac])C1([H])O.[H]C1OC(CO)[C@]([H])(O)C([H])(O)C1([H])[Y].[H]C1OC([H])(CO)[C@]([H])(O)C([H])(O)C1([H])OC1(C)OC([H])(C)[C@]([H])(O)C([H])(O)C1([H])O NDCKPDXOQVCDRH-FHNHQRAVSA-N 0.000 description 1
- HNMSYFYNEIDXMN-WLTXMMDXSA-N C.O.[H]C1C([H])(CO)OC([H])C([H])(N[Ac])C1([H])O.[H]C1OC([H])(CO)[C@]([H])(O)C([H])(O)C1([H])OC1([H])OC([H])(C)[C@]([H])(O)C([H])(O)O1([H])O Chemical compound C.O.[H]C1C([H])(CO)OC([H])C([H])(N[Ac])C1([H])O.[H]C1OC([H])(CO)[C@]([H])(O)C([H])(O)C1([H])OC1([H])OC([H])(C)[C@]([H])(O)C([H])(O)O1([H])O HNMSYFYNEIDXMN-WLTXMMDXSA-N 0.000 description 1
- WKWHSLQZDPWCRR-IPZCTEOASA-N C/N=N/C(=O)COC(O)O.CC Chemical compound C/N=N/C(=O)COC(O)O.CC WKWHSLQZDPWCRR-IPZCTEOASA-N 0.000 description 1
- ODOLEUWXXOOOKC-UHFFFAOYSA-N C1CO1.CN(C)N.CN(C)NC(=O)NC1=CC=CC=C1.C[N+](C)(C)[N-]C(=O)NC1=CC=CC=C1.O=C=NC1=CC=CC=C1 Chemical compound C1CO1.CN(C)N.CN(C)NC(=O)NC1=CC=CC=C1.C[N+](C)(C)[N-]C(=O)NC1=CC=CC=C1.O=C=NC1=CC=CC=C1 ODOLEUWXXOOOKC-UHFFFAOYSA-N 0.000 description 1
- BXWSFXQMBMRKBG-UHFFFAOYSA-N C1OC1[Y]C1CO1 Chemical compound C1OC1[Y]C1CO1 BXWSFXQMBMRKBG-UHFFFAOYSA-N 0.000 description 1
- PEDOORBGWLGHCA-UHFFFAOYSA-N C=CCC(=O)[N-][N+](C)(C)CC(O)CC(=O)[N-][N+](C)(C)CC(C)O Chemical compound C=CCC(=O)[N-][N+](C)(C)CC(O)CC(=O)[N-][N+](C)(C)CC(C)O PEDOORBGWLGHCA-UHFFFAOYSA-N 0.000 description 1
- VNXPFJOXSWOFAU-UHFFFAOYSA-N C=CCC(=O)[N-][N+](C)(C)CC(O)CC(=O)[N-][N+](C)(C)CCO Chemical compound C=CCC(=O)[N-][N+](C)(C)CC(O)CC(=O)[N-][N+](C)(C)CCO VNXPFJOXSWOFAU-UHFFFAOYSA-N 0.000 description 1
- NBCJKDSVYLJHHU-UHFFFAOYSA-N CC(=O)NN(C)(C)C Chemical compound CC(=O)NN(C)(C)C NBCJKDSVYLJHHU-UHFFFAOYSA-N 0.000 description 1
- WFJUAAYWZNSEJD-UHFFFAOYSA-N CC(=O)NN(C)(C)C.CC(=O)NN(C)C Chemical compound CC(=O)NN(C)(C)C.CC(=O)NN(C)C WFJUAAYWZNSEJD-UHFFFAOYSA-N 0.000 description 1
- JYFAMDLJBOZOIC-GMUIIQOCSA-N CC(=O)[N-][N+](C)(C)[Rn].CC[N@@+](C)([N-]C(=O)C[N+](C)(C)[N-]C=O)C1=CC=CC=C1 Chemical compound CC(=O)[N-][N+](C)(C)[Rn].CC[N@@+](C)([N-]C(=O)C[N+](C)(C)[N-]C=O)C1=CC=CC=C1 JYFAMDLJBOZOIC-GMUIIQOCSA-N 0.000 description 1
- ATPGWQJPAPSPRK-FXMYHANSSA-N CC(=O)[N-][N+](C)(C)[Rn].[H][C@@](C)(O)CC1=CC=C([N-][N+](C)(C)C[C@]([H])(C)O)C=C1 Chemical compound CC(=O)[N-][N+](C)(C)[Rn].[H][C@@](C)(O)CC1=CC=C([N-][N+](C)(C)C[C@]([H])(C)O)C=C1 ATPGWQJPAPSPRK-FXMYHANSSA-N 0.000 description 1
- MUICVJBNPVHSEZ-UHFFFAOYSA-N CC(=O)[N-][NH+](C)C.C[N+](C)(C)[N-]C=O Chemical compound CC(=O)[N-][NH+](C)C.C[N+](C)(C)[N-]C=O MUICVJBNPVHSEZ-UHFFFAOYSA-N 0.000 description 1
- OKNKVDMLJQLCCC-UHFFFAOYSA-N CC(C)O[Si](C)(C)C.CN(C)N Chemical compound CC(C)O[Si](C)(C)C.CN(C)N OKNKVDMLJQLCCC-UHFFFAOYSA-N 0.000 description 1
- MINCDBQKWROZJI-UHFFFAOYSA-O CC(C)[N+](C)(C)NC(=O)C1=CC=CC=C1 Chemical compound CC(C)[N+](C)(C)NC(=O)C1=CC=CC=C1 MINCDBQKWROZJI-UHFFFAOYSA-O 0.000 description 1
- DPFRYZDOIZHNNU-UHFFFAOYSA-N CC([O-])=N[N+](C)(C)C.CN(C)C.CN=C=O Chemical compound CC([O-])=N[N+](C)(C)C.CN(C)C.CN=C=O DPFRYZDOIZHNNU-UHFFFAOYSA-N 0.000 description 1
- AHSHBIDZXWXKGH-QXNVWCPVSA-N CC.CC.[H][C@@](O)(C(=O)[N-][N+](C)(C)CC(C)O)[C@]([H])(O)C(=O)N[N+](C)(C)C[C@]([H])(O)[Y][C@]([H])(O)[N+](C)(C)[N-]C(=O)C(C)(C)C Chemical compound CC.CC.[H][C@@](O)(C(=O)[N-][N+](C)(C)CC(C)O)[C@]([H])(O)C(=O)N[N+](C)(C)C[C@]([H])(O)[Y][C@]([H])(O)[N+](C)(C)[N-]C(=O)C(C)(C)C AHSHBIDZXWXKGH-QXNVWCPVSA-N 0.000 description 1
- YVEWMTDTCRHYSX-UHFFFAOYSA-N CC.C[N+](C)(C)CC1CO1.[Cl-] Chemical compound CC.C[N+](C)(C)CC1CO1.[Cl-] YVEWMTDTCRHYSX-UHFFFAOYSA-N 0.000 description 1
- NNLAQYAWURKLQF-QYQBPCCFSA-N CCC(=O)OC.CCC(=O)[N-][N@@+](C)(CCO)C1=CC=CC=C1.C[N@+](N)(CCO)C1=CC=CC=C1.[I-] Chemical compound CCC(=O)OC.CCC(=O)[N-][N@@+](C)(CCO)C1=CC=CC=C1.C[N@+](N)(CCO)C1=CC=CC=C1.[I-] NNLAQYAWURKLQF-QYQBPCCFSA-N 0.000 description 1
- ZSGJFRBYQJIRCK-ALLBUHFWSA-O CCC(CC(C)C(=O)N[N@+](C)(CC)CCO)C1=CC=CC=C1 Chemical compound CCC(CC(C)C(=O)N[N@+](C)(CC)CCO)C1=CC=CC=C1 ZSGJFRBYQJIRCK-ALLBUHFWSA-O 0.000 description 1
- QBJWYMFTMJFGOL-UHFFFAOYSA-N CCCCCCCCCCCCCCCCC1CO1 Chemical compound CCCCCCCCCCCCCCCCC1CO1 QBJWYMFTMJFGOL-UHFFFAOYSA-N 0.000 description 1
- ILMOXHPGXSWIFU-UHFFFAOYSA-N CCCCCCCCCCCCCCCCOC(CCCCCCCCCCCCCCCC)C[N+](C)(C)[N-]C(C)=O Chemical compound CCCCCCCCCCCCCCCCOC(CCCCCCCCCCCCCCCC)C[N+](C)(C)[N-]C(C)=O ILMOXHPGXSWIFU-UHFFFAOYSA-N 0.000 description 1
- NJULPDJJCUEONS-UHFFFAOYSA-N CCOOCCCC[N+](C)(C)[N-]C(=O)CCl.CCOOCCCC[N+](C)(C)[N-]C(=O)C[N+](C)(C)[N-]C(=O)CCl.CN(C)N Chemical compound CCOOCCCC[N+](C)(C)[N-]C(=O)CCl.CCOOCCCC[N+](C)(C)[N-]C(=O)C[N+](C)(C)[N-]C(=O)CCl.CN(C)N NJULPDJJCUEONS-UHFFFAOYSA-N 0.000 description 1
- NSQWVOZKZOZEOX-FQEVSTJZSA-N CC[N@+](C)([N-]C(=O)C[N+](C)(C)[N-]C(=O)CBr)C1=CC=CC=C1 Chemical compound CC[N@+](C)([N-]C(=O)C[N+](C)(C)[N-]C(=O)CBr)C1=CC=CC=C1 NSQWVOZKZOZEOX-FQEVSTJZSA-N 0.000 description 1
- VXAOCWYMTPSWGD-UHFFFAOYSA-N CN(C)(C)[N-]C(=O)CCl Chemical compound CN(C)(C)[N-]C(=O)CCl VXAOCWYMTPSWGD-UHFFFAOYSA-N 0.000 description 1
- DGEMWJMQJGFRGY-UHFFFAOYSA-N CN(C)N.CN(C)N.CN(C)N Chemical compound CN(C)N.CN(C)N.CN(C)N DGEMWJMQJGFRGY-UHFFFAOYSA-N 0.000 description 1
- VTHFATYBWBUJIR-QMTHFTBMSA-P CN(C)N.C[C@H]1CO1.[H][C@@](C)(O)C[N+]([H])(C)C.[H][C@@](C)(O)C[N+]([H])(C)C Chemical compound CN(C)N.C[C@H]1CO1.[H][C@@](C)(O)C[N+]([H])(C)C.[H][C@@](C)(O)C[N+]([H])(C)C VTHFATYBWBUJIR-QMTHFTBMSA-P 0.000 description 1
- YGDROUONTVNYOT-ZGLDZKSDSA-N CN(C)N.[H][C@@](C)(O)CC(=O)OC.[H][C@@](C)(O)CC(=O)[N-][N+](C)(C)C[C@]([H])(C)O.[H][C@]1(C)CO1 Chemical compound CN(C)N.[H][C@@](C)(O)CC(=O)OC.[H][C@@](C)(O)CC(=O)[N-][N+](C)(C)C[C@]([H])(C)O.[H][C@]1(C)CO1 YGDROUONTVNYOT-ZGLDZKSDSA-N 0.000 description 1
- DNCGLJOQBSMSHC-BUAQIUMISA-P COC(=O)C1=CC=C(CC2CO2)C=C1.[H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC=C(C[C@H]2CO2)C=C1.[H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC=C(C[C@H]2CO2)C=C1.[H][C@@](C)(O)C[N+]([H])(C)C.[H][C@@](C)(O)C[N+]([H])(C)C Chemical compound COC(=O)C1=CC=C(CC2CO2)C=C1.[H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC=C(C[C@H]2CO2)C=C1.[H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC=C(C[C@H]2CO2)C=C1.[H][C@@](C)(O)C[N+]([H])(C)C.[H][C@@](C)(O)C[N+]([H])(C)C DNCGLJOQBSMSHC-BUAQIUMISA-P 0.000 description 1
- VUULDJNTOTUGOH-UHFFFAOYSA-O CO[Na].C[N+](C)(C)N.[H][N+](C)(C)C Chemical compound CO[Na].C[N+](C)(C)N.[H][N+](C)(C)C VUULDJNTOTUGOH-UHFFFAOYSA-O 0.000 description 1
- CEPPALOVJZIOCL-ZETCQYMHSA-N C[N-][N@@+](C)([Rn])CC(C)=O Chemical compound C[N-][N@@+](C)([Rn])CC(C)=O CEPPALOVJZIOCL-ZETCQYMHSA-N 0.000 description 1
- ZJESDLRXLBTODG-OVVLOGLBSA-M O.O.O.O.[H]C(O)(/C=C/C)C([H])(C)=O.[H]C(O)(CO)C([H])(O)C1([H])OC(OC)(C(=O)[O-])C([H])([H])C([H])(O)[C@@]1([H])N[Ac].[H]C1C([H])C([H])(O)C([H])OC1([H])CO.[H]C1OC([H])(CO)C([H])C([H])(O)C1([H])O.[H]C1OC([H])(CO)[C@]([H])(O)C([H])(O)C1([H])O.[H]C1OC([H])(CO)[C@]([H])(O)C([H])C1([H])N[Ac] Chemical compound O.O.O.O.[H]C(O)(/C=C/C)C([H])(C)=O.[H]C(O)(CO)C([H])(O)C1([H])OC(OC)(C(=O)[O-])C([H])([H])C([H])(O)[C@@]1([H])N[Ac].[H]C1C([H])C([H])(O)C([H])OC1([H])CO.[H]C1OC([H])(CO)C([H])C([H])(O)C1([H])O.[H]C1OC([H])(CO)[C@]([H])(O)C([H])(O)C1([H])O.[H]C1OC([H])(CO)[C@]([H])(O)C([H])C1([H])N[Ac] ZJESDLRXLBTODG-OVVLOGLBSA-M 0.000 description 1
- VLNHIIYXSPNLKZ-UHFFFAOYSA-N O=C=NCOC(O)O Chemical compound O=C=NCOC(O)O VLNHIIYXSPNLKZ-UHFFFAOYSA-N 0.000 description 1
- SGJAALZBFFPOJN-NRWPOFLRSA-N [H]C(O)(C[N+](C)(C)[N-]C(=O)[C@@](CC)(CC1=CC=CC=C1)NC(=O)CCSC)C1=CC=CC=C1 Chemical compound [H]C(O)(C[N+](C)(C)[N-]C(=O)[C@@](CC)(CC1=CC=CC=C1)NC(=O)CCSC)C1=CC=CC=C1 SGJAALZBFFPOJN-NRWPOFLRSA-N 0.000 description 1
- ZTECNCQUTWLNRZ-UHFFFAOYSA-N [H]C1(CC(=O)OC)OC([H])(OP)C([H])(OP)C([H])(OP)C1([H])OP.[H]C1(C[N+](C)(C)N)OC([H])(OP)C([H])(OP)C([H])(OP)C1([H])OP.[H]C1(O)CC([H])(CC(=O)[N-][N+](C)(C)CC2([H])OC([H])(O)C([H])(O)C([H])(O)C2([H])O)C([H])(O)C([H])(O)C1([H])O Chemical compound [H]C1(CC(=O)OC)OC([H])(OP)C([H])(OP)C([H])(OP)C1([H])OP.[H]C1(C[N+](C)(C)N)OC([H])(OP)C([H])(OP)C([H])(OP)C1([H])OP.[H]C1(O)CC([H])(CC(=O)[N-][N+](C)(C)CC2([H])OC([H])(O)C([H])(O)C([H])(O)C2([H])O)C([H])(O)C([H])(O)C1([H])O ZTECNCQUTWLNRZ-UHFFFAOYSA-N 0.000 description 1
- QZHXJCNYOYUTBU-SXONSRATSA-P [H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC([C@]([H])(O)C[N+]([H])(C)C)=CC=C1.[H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC=C(C[C@]([H])(O)C[N+]([H])(C)C)C=C1 Chemical compound [H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC([C@]([H])(O)C[N+]([H])(C)C)=CC=C1.[H][C@@](C)(O)C[N+](C)(C)[N-]C(=O)C1=CC=C(C[C@]([H])(O)C[N+]([H])(C)C)C=C1 QZHXJCNYOYUTBU-SXONSRATSA-P 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/40—Hydrazines having nitrogen atoms of hydrazine groups being quaternised
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
- C07D209/16—Tryptamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D489/00—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
- C07K1/047—Simultaneous synthesis of different peptide species; Peptide libraries
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biophysics (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Peptides Or Proteins (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/426,547 US6271195B1 (en) | 1992-06-30 | 1999-10-22 | Aminimide-containing molecules and materials as molecular recognition agents |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90677092A | 1992-06-30 | 1992-06-30 | |
US90676992A | 1992-06-30 | 1992-06-30 | |
US4155993A | 1993-04-02 | 1993-04-02 | |
US08/204,206 US5705585A (en) | 1993-06-30 | 1993-06-30 | Aminimide-containing molecules and materials as molecular recognition agents |
US08/765,173 US5981467A (en) | 1995-03-27 | 1996-02-16 | Aminimide-containing molecules and materials as molecular recognition agents |
US09/426,547 US6271195B1 (en) | 1992-06-30 | 1999-10-22 | Aminimide-containing molecules and materials as molecular recognition agents |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/765,173 Continuation US5981467A (en) | 1992-06-30 | 1996-02-16 | Aminimide-containing molecules and materials as molecular recognition agents |
Publications (1)
Publication Number | Publication Date |
---|---|
US6271195B1 true US6271195B1 (en) | 2001-08-07 |
Family
ID=22757042
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/204,206 Expired - Fee Related US5705585A (en) | 1992-06-30 | 1993-06-30 | Aminimide-containing molecules and materials as molecular recognition agents |
US08/765,173 Expired - Fee Related US5981467A (en) | 1992-06-30 | 1996-02-16 | Aminimide-containing molecules and materials as molecular recognition agents |
US09/426,547 Expired - Fee Related US6271195B1 (en) | 1992-06-30 | 1999-10-22 | Aminimide-containing molecules and materials as molecular recognition agents |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/204,206 Expired - Fee Related US5705585A (en) | 1992-06-30 | 1993-06-30 | Aminimide-containing molecules and materials as molecular recognition agents |
US08/765,173 Expired - Fee Related US5981467A (en) | 1992-06-30 | 1996-02-16 | Aminimide-containing molecules and materials as molecular recognition agents |
Country Status (1)
Country | Link |
---|---|
US (3) | US5705585A (US06271195-20010807-C00083.png) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050186685A1 (en) * | 2004-01-17 | 2005-08-25 | Gyros Ab | Protecting agent |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5705585A (en) * | 1993-06-30 | 1998-01-06 | Arqule, Inc. | Aminimide-containing molecules and materials as molecular recognition agents |
DE19741335C1 (de) * | 1997-09-19 | 1999-06-10 | Bosch Gmbh Robert | Sensormembran einer Optode sowie Verfahren, Vorrichtung und deren Verwendung zur Bestimmung von Gasen in Gasgemischen |
CN1058722C (zh) * | 1998-12-29 | 2000-11-22 | 四川省天然药物研究所 | 一种新型重金属促排剂的制备方法及其用于治疗和预防重金属中毒的用途 |
BR0007532A (pt) * | 1999-01-13 | 2001-11-20 | Univ New York State Res Found | Métodos para identificar inibidores de proteìnaquinase, para testar compostos para umacapacidade de inibir a atividade de proteìnaquinase e para inibir uma proteìna quinase, inibidorde proteìna tirosina quinase não peptìdica, e,método de tratar uma condição responsiva a uminibidor de proteìna quinase em um paciente |
US7070936B1 (en) * | 1999-01-13 | 2006-07-04 | The Research Foundation Of State University Of New York | Method for designing protein kinase inhibitors |
CA2383094A1 (en) * | 2001-04-24 | 2002-10-24 | Nitech S.A. | Electrochemical cell |
WO2003035621A1 (en) * | 2001-10-22 | 2003-05-01 | The Research Foundation Of State University Of New York | Protein kinase and phosphatase inhibitors, methods for designing them, and methods of using them |
US7005445B2 (en) * | 2001-10-22 | 2006-02-28 | The Research Foundation Of State University Of New York | Protein kinase and phosphatase inhibitors and methods for designing them |
US8845927B2 (en) | 2006-06-02 | 2014-09-30 | Qd Vision, Inc. | Functionalized nanoparticles and method |
US9297092B2 (en) | 2005-06-05 | 2016-03-29 | Qd Vision, Inc. | Compositions, optical component, system including an optical component, devices, and other products |
US8849087B2 (en) | 2006-03-07 | 2014-09-30 | Qd Vision, Inc. | Compositions, optical component, system including an optical component, devices, and other products |
US9212056B2 (en) | 2006-06-02 | 2015-12-15 | Qd Vision, Inc. | Nanoparticle including multi-functional ligand and method |
US7838542B2 (en) * | 2006-06-29 | 2010-11-23 | Kinex Pharmaceuticals, Llc | Bicyclic compositions and methods for modulating a kinase cascade |
US8124598B2 (en) | 2006-09-14 | 2012-02-28 | Sharon Sageman | 7-keto DHEA for psychiatric use |
US20100160274A1 (en) * | 2007-09-07 | 2010-06-24 | Sharon Sageman | 7-KETO DHEA for Psychiatric Use |
US10351661B2 (en) | 2015-12-10 | 2019-07-16 | Ppg Industries Ohio, Inc. | Method for producing an aminimide |
US10377928B2 (en) | 2015-12-10 | 2019-08-13 | Ppg Industries Ohio, Inc. | Structural adhesive compositions |
Citations (112)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1809950U (de) | 1959-12-29 | 1960-04-21 | Kabelwerke Reinshagen G M B H | Isolierte elektrische leitung. |
FR1478953A (fr) | 1965-05-06 | 1967-04-28 | Hoechst Ag | Nouveaux benzène-sulfonyl-semicarbazides et leur préparation |
US3410880A (en) | 1963-10-30 | 1968-11-12 | Procter & Gamble | N-trialkylammonium imides of higher fatty acids |
FR1558886A (US06271195-20010807-C00083.png) | 1967-04-05 | 1969-02-28 | ||
US3450673A (en) | 1965-09-07 | 1969-06-17 | Ashland Oil Inc | Polyurethane compositions from diaminimides |
US3485806A (en) | 1968-02-07 | 1969-12-23 | Ashland Oil Inc | Hydroxy substituted aminimides |
US3488327A (en) | 1967-06-30 | 1970-01-06 | Roehm & Haas Gmbh | Preparation of coating materials |
US3488389A (en) | 1965-09-07 | 1970-01-06 | Ashland Oil Inc | Perfluoroimides |
GB1181218A (en) | 1965-12-17 | 1970-02-11 | Ashland Oil Inc | Substituted Aminimides, their Preparation and Rearrangement to Form Isocyanates |
US3499032A (en) | 1967-04-25 | 1970-03-03 | Ashland Oil Inc | Hydroxyl-,mercapto-,and amino-substituted aminimides |
US3511894A (en) | 1966-09-10 | 1970-05-12 | Roehm & Haas Gmbh | Graft polymers and preparation thereof |
US3527802A (en) | 1967-05-05 | 1970-09-08 | Ashland Oil Inc | Acrylic aminimides |
US3555095A (en) | 1968-03-19 | 1971-01-12 | Ashland Oil Inc | Hydroxy aminimines |
US3565868A (en) | 1968-03-19 | 1971-02-23 | Ashland Oil Inc | Polymers of unsymmetrical disubstituted hydrazine |
US3567725A (en) | 1968-11-20 | 1971-03-02 | Merck & Co Inc | Process for preparation of 1h-imidazo-(4,5-b)pyrazin-2-ones |
US3583950A (en) | 1967-06-30 | 1971-06-08 | Roehm & Haas Gmbh | Azlactone copolymers |
US3598790A (en) | 1966-07-01 | 1971-08-10 | Roehm & Haas Gmbh | Azlactone copolymers |
US3641145A (en) | 1967-08-23 | 1972-02-08 | Ashland Oil Inc | Vinyl aromatic aminimides |
US3664990A (en) | 1967-05-05 | 1972-05-23 | Ashland Oil Inc | Acrylic aminimides and polymers thereof |
US3671473A (en) | 1968-03-19 | 1972-06-20 | Ashland Oil Inc | Polymers formed from the reaction of a mixture of a polyepoxide and a polyester and an unsymmetrical disubstituted hydrazine |
US3676453A (en) | 1968-11-07 | 1972-07-11 | Merck & Co Inc | Oxazole and oxazol-5-one derivatives |
GB1284304A (en) | 1968-11-20 | 1972-08-09 | Basf Ag | Substituted hydrazine derivatives and agents containing them for retarding the growth of plants |
US3704128A (en) | 1969-03-14 | 1972-11-28 | Konishiroku Photo Ind | N-ylide compounds as antistatic agents in photography |
US3706797A (en) | 1969-08-06 | 1972-12-19 | Ashland Oil Inc | Bisacyl aminimides |
US3706800A (en) | 1970-02-26 | 1972-12-19 | Ashland Oil Inc | Process for the preparation of aminimides |
US3715343A (en) | 1971-08-11 | 1973-02-06 | Ashland Oil Inc | Polymers of vinyl aminimides |
US3728387A (en) | 1972-03-17 | 1973-04-17 | Ashland Oil Inc | Acrylamide of methacrylamide monomer with n-substituted amininmide residues |
US3756994A (en) | 1967-08-23 | 1973-09-04 | Ashland Oil Inc | Vinyl aromatic aminimides and polymers thereof |
US3781319A (en) | 1970-09-28 | 1973-12-25 | Univ Iowa | Process for preparing isocyanates |
US3794495A (en) | 1970-12-18 | 1974-02-26 | Konishiroku Photo Ind | Prevention of static in light-sensitive photographic materials using bisaminimide compounds |
US3803220A (en) | 1971-03-02 | 1974-04-09 | Kendall & Co | Mono aminimide derivatives of unsaturated dicarboxylic acids |
US3811887A (en) | 1970-12-18 | 1974-05-21 | Konishiroku Photo Ind | Photographic material comprising bisacylhydrazinium compounds |
US3818065A (en) | 1971-12-22 | 1974-06-18 | Basf Ag | Production of aminoacid precursors |
US3828007A (en) | 1972-02-18 | 1974-08-06 | Ashland Oil Inc | Process of reacting isocyanate or isothiocyanate and compositions therefor |
US3850969A (en) | 1971-05-28 | 1974-11-26 | Ashland Oil Inc | Process for the preparation of hydroxy substituted aminimides |
US3893974A (en) | 1971-04-20 | 1975-07-08 | Permachem Asia Co Ltd | Epoxy resin compositions containing aminimide compound |
US3898087A (en) | 1974-06-14 | 1975-08-05 | Ball Corp | Photopolymerizable compositions containing aminimides |
US3904749A (en) | 1971-10-22 | 1975-09-09 | Ashland Oil Inc | Hair setting preparations |
US3925284A (en) | 1974-06-24 | 1975-12-09 | Upjohn Co | Polyisocyanate-based foam process using aminimides as catalyst |
US3934031A (en) | 1974-04-29 | 1976-01-20 | Michigan State University | Certain aminimides used to control bacteria and fungi |
US3934029A (en) | 1974-04-29 | 1976-01-20 | Michigan State University | Certain aminimides used to control bacteria and fungi |
US3934035A (en) | 1974-04-29 | 1976-01-20 | Michigan State University | Certain aminimides used to control bacteria and fungi |
US3946131A (en) | 1974-05-06 | 1976-03-23 | Owens-Corning Fiberglas Corporation | Glass fibers coated with silicon containing aminimide compounds |
US3948866A (en) | 1970-02-27 | 1976-04-06 | Rohm Gmbh | Polymerization with the aid of macromolecule having both a monomer soluble portion and suspension soluble portion |
US3963776A (en) | 1974-06-24 | 1976-06-15 | E. I. Du Pont De Nemours And Company | Amine fluoroacylimide surfactants |
US3963703A (en) | 1971-09-13 | 1976-06-15 | Ashland Oil, Inc. | Trialkylammonium -N-[β(1-aziridinyl)] propionoylimines |
US3968065A (en) | 1974-12-30 | 1976-07-06 | The B. F. Goodrich Company | Vulcanizable polymer blends of a halogen-containing polymer and a carboxyl-containing polymer |
US3969298A (en) | 1973-08-24 | 1976-07-13 | The Kendall Company | Selected lipophilic aminimides and polymers derived therefrom useful for making stable emulsions |
US3983166A (en) | 1974-03-18 | 1976-09-28 | The Kendall Company | Monomeric emulsion stabilizers |
US3985807A (en) | 1975-03-31 | 1976-10-12 | Ashland Oil, Inc. | Alkoxy derivatives of hydroxy aminimides |
US4005055A (en) | 1975-05-22 | 1977-01-25 | Skeist Laboratories, Incorporated | Anaerobic aminimide curing compositions |
US4016340A (en) | 1975-08-07 | 1977-04-05 | Polaroid Corporation | Hydroxyl-containing polymers having aminimide groups attached thereto through an ether linkage |
US4022623A (en) | 1975-10-28 | 1977-05-10 | Polaroid Corporation | Photosensitive emulsion containing polyvinyl aminimide polymers |
US4046658A (en) | 1975-08-15 | 1977-09-06 | General Motors Corporation | Process for electrocoating aminimide containing compositions |
US4067830A (en) | 1976-03-29 | 1978-01-10 | Ashland Oil, Inc. | Catalytic trimerization of polyisocyanates |
US4070348A (en) | 1973-07-25 | 1978-01-24 | Rohm Gmbh | Water-swellable, bead copolymer |
US4078901A (en) | 1976-12-20 | 1978-03-14 | Texaco Inc. | Detergent fuel composition |
US4080206A (en) | 1974-12-30 | 1978-03-21 | Polaroid Corporation | Photographic processing composition containing polyvinyl aminimide |
US4097444A (en) | 1976-03-02 | 1978-06-27 | Hoechst Aktiengesellschaft | Process for the dyeing of water-insoluble thermoplastic polymers and polycondensates in the mass |
US4102916A (en) | 1976-12-02 | 1978-07-25 | Ciba-Geigy Corporation | Perfluoroalkylthioaminimide derivatives |
US4122159A (en) | 1977-02-24 | 1978-10-24 | L'oreal | Aerosol foaming compositions |
US4140680A (en) | 1976-12-22 | 1979-02-20 | Polaroid Corporation | 2-Acrylamido-2-methylpropane sulfonic acid vinyl aminimide/copolymer |
US4162355A (en) | 1976-06-30 | 1979-07-24 | Board Of Regents, For And On Behalf Of The University Of Florida | Copolymers of (a) aminimides and (b) vinyl pendant primary halomethy monomers useful for affinity chromatography |
US4189481A (en) | 1975-11-18 | 1980-02-19 | Michigan State University | Antimicrobial compositions |
US4212905A (en) | 1976-06-30 | 1980-07-15 | Board of Reagents, for and on behalf of the University of Florida | Method of coating supports using addition copolymers of aminimides |
US4213860A (en) | 1976-06-30 | 1980-07-22 | Board of Regents, State of Florida for and on behalf of the University of Florida | Affinity chromatography and substrate useful therefor |
US4217364A (en) | 1975-11-18 | 1980-08-12 | Michigan State University | Antimicrobial compositions |
US4260705A (en) | 1976-06-30 | 1981-04-07 | Board Of Regents, For And On Behalf Of The University Of Florida | Addition copolymers of aminimides useful for affinity chromatography |
US4280008A (en) | 1976-12-24 | 1981-07-21 | Basf Aktiengesellschaft | Chirally substituted 2-imidazolin-5-ones |
US4304705A (en) | 1980-01-02 | 1981-12-08 | Minnesota Mining And Manufacturing Company | Radiation-curable polymers containing pendant unsaturated peptide groups derived from azlactone polymers |
US4378411A (en) | 1980-01-02 | 1983-03-29 | Minnesota Mining And Manufacturing Company | Radiation-curable polymers |
US4424272A (en) | 1981-08-03 | 1984-01-03 | Polaroid Corporation | Temporary polymeric mordants and elements containing same |
US4451619A (en) | 1982-09-30 | 1984-05-29 | Minnesota Mining And Manufacturing Company | Method of hydrophilizing or hydrophobizing polymers |
US4485236A (en) | 1982-09-27 | 1984-11-27 | Minnesota Mining And Manufacturing Company | Azlactone-functional compounds |
US4548981A (en) | 1983-07-01 | 1985-10-22 | Polaroid Corporation | Compositions and articles containing polymeric vinyl aromatic aminimides |
US4563467A (en) | 1983-02-15 | 1986-01-07 | Provesan S.A. | Derivatives of N-iminopyridinium betaines having anti-hypertensive and salidiuretic activity and their preparation |
US4617253A (en) | 1984-06-06 | 1986-10-14 | Polaroid Corporation | Polymeric pyridinium ylides and products prepared from same |
US4624995A (en) | 1985-04-09 | 1986-11-25 | Minnesota Mining And Manufacturing Company | Triazolinethione-containing polymer |
US4645711A (en) | 1985-08-26 | 1987-02-24 | Minnesota Mining And Manufacturing Company | Removable pressure-sensitive adhesive tape |
US4667012A (en) | 1984-12-14 | 1987-05-19 | Minnesota Mining And Manufacturing Company | Imidazolinone-containing polymer and copolymer |
US4695608A (en) | 1984-03-29 | 1987-09-22 | Minnesota Mining And Manufacturing Company | Continuous process for making polymers having pendant azlactone or macromolecular moieties |
US4705824A (en) | 1986-02-14 | 1987-11-10 | W. R. Grace & Co. | Poly(5-imidazolone) and process therefor |
US4737560A (en) | 1987-03-13 | 1988-04-12 | Minnesota Mining And Manufacturing Company | Polymer beads |
US4740568A (en) | 1985-04-09 | 1988-04-26 | Minnesota Mining And Manufacturing Company | Triazolinethione-containing polymer |
US4777217A (en) | 1987-02-26 | 1988-10-11 | Minnesota Mining And Manufacturing Company | Methacrylamide functional polymers and method |
US4777276A (en) | 1981-10-29 | 1988-10-11 | Minnesota Mining And Manufacturing Company | Acrylamidoacylated oligomers |
EP0212617B1 (en) | 1985-08-23 | 1989-01-11 | Lederle (Japan) Ltd. | Process for producing 4-biphenylylacetic acid |
US4816554A (en) | 1987-05-27 | 1989-03-28 | Minnesota Mining And Manufacturing Company | Poly(amido methyl-benzazole) |
US4841021A (en) | 1987-11-30 | 1989-06-20 | Minnesota Mining And Manufacturing Company | Polypyridinium |
US4852969A (en) | 1988-03-17 | 1989-08-01 | Minnesota Mining And Manufacturing Company | Silyl 2-amidoacetate and silyl 3-amidopropionate compositions and optical fiber made therefrom |
US4871824A (en) | 1987-03-13 | 1989-10-03 | Minnesota Mining And Manufacturing Company | Variably crosslinked polymeric supports |
US4874822A (en) | 1988-04-07 | 1989-10-17 | Minnesota Mining And Manufacturing Company | Process for the acrylamidoacylation of alcohols |
US4898923A (en) | 1987-11-30 | 1990-02-06 | Minnesota Mining And Manufacturing Company | Polypyridinium copolymer |
US4948715A (en) | 1988-02-15 | 1990-08-14 | Minnesota Mining And Manufacturing Company | Polymeric polymethine dyes and optical data storage media containing same |
US4981933A (en) | 1989-06-23 | 1991-01-01 | Polaroid Corporation | Azlactone copolymers |
US5013795A (en) | 1989-04-10 | 1991-05-07 | Minnesota Mining And Manufacturing Company | Azlactone graft copolymers |
US5039813A (en) | 1990-06-29 | 1991-08-13 | Polaroid Corporation | 2-(4-alkenylphenyl)-5-oxazolones and polymers thereof |
US5066559A (en) | 1990-01-22 | 1991-11-19 | Minnesota Mining And Manufacturing Company | Liquid electrophotographic toner |
US5075352A (en) | 1989-08-15 | 1991-12-24 | Minnesota Mining And Manufacturing Company | Stabilized polymeric dispersions |
US5081197A (en) | 1990-10-23 | 1992-01-14 | Minnesota Mining And Manufacturing Company | Oligo(2-alkenyl azlactones) |
US5091489A (en) | 1990-10-23 | 1992-02-25 | Minnesota Mining And Manufacturing Company | Oligo (2-alkenyl azlactones) |
US5094766A (en) | 1990-07-02 | 1992-03-10 | Texaco Inc. | Dispersant-antioxidant viscosity index improver |
US5138071A (en) | 1988-09-17 | 1992-08-11 | Basf Aktiengesellschaft | Process for preparing peptides with n-terminal non-proteinogenous amino acids |
US5147957A (en) | 1989-09-22 | 1992-09-15 | Minnesota Mining And Manufacturing Company | Hydrosilated azlactone functional silicon containing compounds and derivatives thereof |
US5149806A (en) | 1990-03-28 | 1992-09-22 | Minnesota Mining And Manufacturing Company | Azlactone michael adducts |
US5157108A (en) | 1989-12-12 | 1992-10-20 | Minnesota Mining And Manufacturing Company | Thermally sensitive linkages |
US5157145A (en) | 1988-09-17 | 1992-10-20 | Basf Aktiengesellschaft | Process for the preparation of dipeptides with c-terminal non-proteinogenous amino acids |
US5175081A (en) | 1990-08-31 | 1992-12-29 | Minnesota Mining And Manufacturing Company | Post-processsing stabilization of photothermographic emulsions |
US5185102A (en) | 1989-06-08 | 1993-02-09 | Minnesota Mining And Manufacturing Company | Polymeric charge transfer complexes for nonlinear optical applications |
US5194623A (en) | 1990-08-31 | 1993-03-16 | Minnesota Mining And Manufacturing Company | Azlactone based photographic reagents |
US5200471A (en) | 1990-11-05 | 1993-04-06 | Minnesota Mining And Manufacturing Company | Biomolecules covalently immobilized with a high bound specific biological activity and method of preparing same |
US5981467A (en) * | 1995-03-27 | 1999-11-09 | Arqule, Inc. | Aminimide-containing molecules and materials as molecular recognition agents |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3949140A (en) * | 1974-05-06 | 1976-04-06 | Owens-Corning Fiberglas Corporation | Organo silicon derivatives coated on glass fibers |
-
1993
- 1993-06-30 US US08/204,206 patent/US5705585A/en not_active Expired - Fee Related
-
1996
- 1996-02-16 US US08/765,173 patent/US5981467A/en not_active Expired - Fee Related
-
1999
- 1999-10-22 US US09/426,547 patent/US6271195B1/en not_active Expired - Fee Related
Patent Citations (117)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1809950U (de) | 1959-12-29 | 1960-04-21 | Kabelwerke Reinshagen G M B H | Isolierte elektrische leitung. |
US3410880A (en) | 1963-10-30 | 1968-11-12 | Procter & Gamble | N-trialkylammonium imides of higher fatty acids |
FR1478953A (fr) | 1965-05-06 | 1967-04-28 | Hoechst Ag | Nouveaux benzène-sulfonyl-semicarbazides et leur préparation |
GB1128382A (en) | 1965-05-06 | 1968-09-25 | Hoechst Ag | New benzene-sulphonyl semicarbazides and preparations containing them |
US3488389A (en) | 1965-09-07 | 1970-01-06 | Ashland Oil Inc | Perfluoroimides |
US3450673A (en) | 1965-09-07 | 1969-06-17 | Ashland Oil Inc | Polyurethane compositions from diaminimides |
GB1181218A (en) | 1965-12-17 | 1970-02-11 | Ashland Oil Inc | Substituted Aminimides, their Preparation and Rearrangement to Form Isocyanates |
US3598790A (en) | 1966-07-01 | 1971-08-10 | Roehm & Haas Gmbh | Azlactone copolymers |
US3511894A (en) | 1966-09-10 | 1970-05-12 | Roehm & Haas Gmbh | Graft polymers and preparation thereof |
FR1558886A (US06271195-20010807-C00083.png) | 1967-04-05 | 1969-02-28 | ||
US3499032A (en) | 1967-04-25 | 1970-03-03 | Ashland Oil Inc | Hydroxyl-,mercapto-,and amino-substituted aminimides |
US3527802A (en) | 1967-05-05 | 1970-09-08 | Ashland Oil Inc | Acrylic aminimides |
US3664990A (en) | 1967-05-05 | 1972-05-23 | Ashland Oil Inc | Acrylic aminimides and polymers thereof |
US3488327A (en) | 1967-06-30 | 1970-01-06 | Roehm & Haas Gmbh | Preparation of coating materials |
US3583950A (en) | 1967-06-30 | 1971-06-08 | Roehm & Haas Gmbh | Azlactone copolymers |
US3641145A (en) | 1967-08-23 | 1972-02-08 | Ashland Oil Inc | Vinyl aromatic aminimides |
US3756994A (en) | 1967-08-23 | 1973-09-04 | Ashland Oil Inc | Vinyl aromatic aminimides and polymers thereof |
GB1265163A (US06271195-20010807-C00083.png) | 1968-02-07 | 1972-03-01 | ||
US3485806A (en) | 1968-02-07 | 1969-12-23 | Ashland Oil Inc | Hydroxy substituted aminimides |
US3565868A (en) | 1968-03-19 | 1971-02-23 | Ashland Oil Inc | Polymers of unsymmetrical disubstituted hydrazine |
US3555095A (en) | 1968-03-19 | 1971-01-12 | Ashland Oil Inc | Hydroxy aminimines |
US3671473A (en) | 1968-03-19 | 1972-06-20 | Ashland Oil Inc | Polymers formed from the reaction of a mixture of a polyepoxide and a polyester and an unsymmetrical disubstituted hydrazine |
US3676453A (en) | 1968-11-07 | 1972-07-11 | Merck & Co Inc | Oxazole and oxazol-5-one derivatives |
US3567725A (en) | 1968-11-20 | 1971-03-02 | Merck & Co Inc | Process for preparation of 1h-imidazo-(4,5-b)pyrazin-2-ones |
GB1284304A (en) | 1968-11-20 | 1972-08-09 | Basf Ag | Substituted hydrazine derivatives and agents containing them for retarding the growth of plants |
US3704128A (en) | 1969-03-14 | 1972-11-28 | Konishiroku Photo Ind | N-ylide compounds as antistatic agents in photography |
US3706797A (en) | 1969-08-06 | 1972-12-19 | Ashland Oil Inc | Bisacyl aminimides |
US3706800A (en) | 1970-02-26 | 1972-12-19 | Ashland Oil Inc | Process for the preparation of aminimides |
US3948866A (en) | 1970-02-27 | 1976-04-06 | Rohm Gmbh | Polymerization with the aid of macromolecule having both a monomer soluble portion and suspension soluble portion |
US3781319A (en) | 1970-09-28 | 1973-12-25 | Univ Iowa | Process for preparing isocyanates |
US3794495A (en) | 1970-12-18 | 1974-02-26 | Konishiroku Photo Ind | Prevention of static in light-sensitive photographic materials using bisaminimide compounds |
US3811887A (en) | 1970-12-18 | 1974-05-21 | Konishiroku Photo Ind | Photographic material comprising bisacylhydrazinium compounds |
US3803220A (en) | 1971-03-02 | 1974-04-09 | Kendall & Co | Mono aminimide derivatives of unsaturated dicarboxylic acids |
US3893974A (en) | 1971-04-20 | 1975-07-08 | Permachem Asia Co Ltd | Epoxy resin compositions containing aminimide compound |
US3850969A (en) | 1971-05-28 | 1974-11-26 | Ashland Oil Inc | Process for the preparation of hydroxy substituted aminimides |
US3715343A (en) | 1971-08-11 | 1973-02-06 | Ashland Oil Inc | Polymers of vinyl aminimides |
US3963703A (en) | 1971-09-13 | 1976-06-15 | Ashland Oil, Inc. | Trialkylammonium -N-[β(1-aziridinyl)] propionoylimines |
US3904749A (en) | 1971-10-22 | 1975-09-09 | Ashland Oil Inc | Hair setting preparations |
US3818065A (en) | 1971-12-22 | 1974-06-18 | Basf Ag | Production of aminoacid precursors |
US3828007A (en) | 1972-02-18 | 1974-08-06 | Ashland Oil Inc | Process of reacting isocyanate or isothiocyanate and compositions therefor |
US3728387A (en) | 1972-03-17 | 1973-04-17 | Ashland Oil Inc | Acrylamide of methacrylamide monomer with n-substituted amininmide residues |
US4070348A (en) | 1973-07-25 | 1978-01-24 | Rohm Gmbh | Water-swellable, bead copolymer |
US3969298A (en) | 1973-08-24 | 1976-07-13 | The Kendall Company | Selected lipophilic aminimides and polymers derived therefrom useful for making stable emulsions |
US3983166A (en) | 1974-03-18 | 1976-09-28 | The Kendall Company | Monomeric emulsion stabilizers |
US3934031A (en) | 1974-04-29 | 1976-01-20 | Michigan State University | Certain aminimides used to control bacteria and fungi |
US3934029A (en) | 1974-04-29 | 1976-01-20 | Michigan State University | Certain aminimides used to control bacteria and fungi |
US3934035A (en) | 1974-04-29 | 1976-01-20 | Michigan State University | Certain aminimides used to control bacteria and fungi |
US3946131A (en) | 1974-05-06 | 1976-03-23 | Owens-Corning Fiberglas Corporation | Glass fibers coated with silicon containing aminimide compounds |
US3898087A (en) | 1974-06-14 | 1975-08-05 | Ball Corp | Photopolymerizable compositions containing aminimides |
US3963776A (en) | 1974-06-24 | 1976-06-15 | E. I. Du Pont De Nemours And Company | Amine fluoroacylimide surfactants |
US3925284A (en) | 1974-06-24 | 1975-12-09 | Upjohn Co | Polyisocyanate-based foam process using aminimides as catalyst |
US4080206A (en) | 1974-12-30 | 1978-03-21 | Polaroid Corporation | Photographic processing composition containing polyvinyl aminimide |
US3968065A (en) | 1974-12-30 | 1976-07-06 | The B. F. Goodrich Company | Vulcanizable polymer blends of a halogen-containing polymer and a carboxyl-containing polymer |
US3985807A (en) | 1975-03-31 | 1976-10-12 | Ashland Oil, Inc. | Alkoxy derivatives of hydroxy aminimides |
US4005055A (en) | 1975-05-22 | 1977-01-25 | Skeist Laboratories, Incorporated | Anaerobic aminimide curing compositions |
US4016340A (en) | 1975-08-07 | 1977-04-05 | Polaroid Corporation | Hydroxyl-containing polymers having aminimide groups attached thereto through an ether linkage |
US4046658A (en) | 1975-08-15 | 1977-09-06 | General Motors Corporation | Process for electrocoating aminimide containing compositions |
US4022623A (en) | 1975-10-28 | 1977-05-10 | Polaroid Corporation | Photosensitive emulsion containing polyvinyl aminimide polymers |
US4217364A (en) | 1975-11-18 | 1980-08-12 | Michigan State University | Antimicrobial compositions |
US4189481A (en) | 1975-11-18 | 1980-02-19 | Michigan State University | Antimicrobial compositions |
US4097444A (en) | 1976-03-02 | 1978-06-27 | Hoechst Aktiengesellschaft | Process for the dyeing of water-insoluble thermoplastic polymers and polycondensates in the mass |
US4067830A (en) | 1976-03-29 | 1978-01-10 | Ashland Oil, Inc. | Catalytic trimerization of polyisocyanates |
US4162355A (en) | 1976-06-30 | 1979-07-24 | Board Of Regents, For And On Behalf Of The University Of Florida | Copolymers of (a) aminimides and (b) vinyl pendant primary halomethy monomers useful for affinity chromatography |
US4212905A (en) | 1976-06-30 | 1980-07-15 | Board of Reagents, for and on behalf of the University of Florida | Method of coating supports using addition copolymers of aminimides |
US4213860A (en) | 1976-06-30 | 1980-07-22 | Board of Regents, State of Florida for and on behalf of the University of Florida | Affinity chromatography and substrate useful therefor |
US4260705A (en) | 1976-06-30 | 1981-04-07 | Board Of Regents, For And On Behalf Of The University Of Florida | Addition copolymers of aminimides useful for affinity chromatography |
US4102916A (en) | 1976-12-02 | 1978-07-25 | Ciba-Geigy Corporation | Perfluoroalkylthioaminimide derivatives |
US4078901A (en) | 1976-12-20 | 1978-03-14 | Texaco Inc. | Detergent fuel composition |
US4140680A (en) | 1976-12-22 | 1979-02-20 | Polaroid Corporation | 2-Acrylamido-2-methylpropane sulfonic acid vinyl aminimide/copolymer |
US4280008A (en) | 1976-12-24 | 1981-07-21 | Basf Aktiengesellschaft | Chirally substituted 2-imidazolin-5-ones |
US4122159A (en) | 1977-02-24 | 1978-10-24 | L'oreal | Aerosol foaming compositions |
US4304705A (en) | 1980-01-02 | 1981-12-08 | Minnesota Mining And Manufacturing Company | Radiation-curable polymers containing pendant unsaturated peptide groups derived from azlactone polymers |
US4378411A (en) | 1980-01-02 | 1983-03-29 | Minnesota Mining And Manufacturing Company | Radiation-curable polymers |
US4424272A (en) | 1981-08-03 | 1984-01-03 | Polaroid Corporation | Temporary polymeric mordants and elements containing same |
US4777276A (en) | 1981-10-29 | 1988-10-11 | Minnesota Mining And Manufacturing Company | Acrylamidoacylated oligomers |
US4485236A (en) | 1982-09-27 | 1984-11-27 | Minnesota Mining And Manufacturing Company | Azlactone-functional compounds |
US4451619A (en) | 1982-09-30 | 1984-05-29 | Minnesota Mining And Manufacturing Company | Method of hydrophilizing or hydrophobizing polymers |
US4563467A (en) | 1983-02-15 | 1986-01-07 | Provesan S.A. | Derivatives of N-iminopyridinium betaines having anti-hypertensive and salidiuretic activity and their preparation |
US4548981A (en) | 1983-07-01 | 1985-10-22 | Polaroid Corporation | Compositions and articles containing polymeric vinyl aromatic aminimides |
US4695608A (en) | 1984-03-29 | 1987-09-22 | Minnesota Mining And Manufacturing Company | Continuous process for making polymers having pendant azlactone or macromolecular moieties |
US4617253A (en) | 1984-06-06 | 1986-10-14 | Polaroid Corporation | Polymeric pyridinium ylides and products prepared from same |
US4670528A (en) | 1984-06-06 | 1987-06-02 | Polaroid Corporation | Polymeric pyridinium ylides and products prepared from same |
US4667012A (en) | 1984-12-14 | 1987-05-19 | Minnesota Mining And Manufacturing Company | Imidazolinone-containing polymer and copolymer |
EP0185493B1 (en) | 1984-12-14 | 1993-07-28 | Minnesota Mining And Manufacturing Company | Imidazolinone-containing polymers and copolymers |
US4785070A (en) | 1984-12-14 | 1988-11-15 | Minnesota Mining And Manufacturing Company | Imidazolinone-containing copolymer |
US4624995A (en) | 1985-04-09 | 1986-11-25 | Minnesota Mining And Manufacturing Company | Triazolinethione-containing polymer |
US4740568A (en) | 1985-04-09 | 1988-04-26 | Minnesota Mining And Manufacturing Company | Triazolinethione-containing polymer |
EP0212617B1 (en) | 1985-08-23 | 1989-01-11 | Lederle (Japan) Ltd. | Process for producing 4-biphenylylacetic acid |
US4645711A (en) | 1985-08-26 | 1987-02-24 | Minnesota Mining And Manufacturing Company | Removable pressure-sensitive adhesive tape |
US4705824A (en) | 1986-02-14 | 1987-11-10 | W. R. Grace & Co. | Poly(5-imidazolone) and process therefor |
US4777217A (en) | 1987-02-26 | 1988-10-11 | Minnesota Mining And Manufacturing Company | Methacrylamide functional polymers and method |
US4871824A (en) | 1987-03-13 | 1989-10-03 | Minnesota Mining And Manufacturing Company | Variably crosslinked polymeric supports |
US4737560A (en) | 1987-03-13 | 1988-04-12 | Minnesota Mining And Manufacturing Company | Polymer beads |
US4816554A (en) | 1987-05-27 | 1989-03-28 | Minnesota Mining And Manufacturing Company | Poly(amido methyl-benzazole) |
US4841021A (en) | 1987-11-30 | 1989-06-20 | Minnesota Mining And Manufacturing Company | Polypyridinium |
US4898923A (en) | 1987-11-30 | 1990-02-06 | Minnesota Mining And Manufacturing Company | Polypyridinium copolymer |
US4948715A (en) | 1988-02-15 | 1990-08-14 | Minnesota Mining And Manufacturing Company | Polymeric polymethine dyes and optical data storage media containing same |
US4852969A (en) | 1988-03-17 | 1989-08-01 | Minnesota Mining And Manufacturing Company | Silyl 2-amidoacetate and silyl 3-amidopropionate compositions and optical fiber made therefrom |
US4874822A (en) | 1988-04-07 | 1989-10-17 | Minnesota Mining And Manufacturing Company | Process for the acrylamidoacylation of alcohols |
US5138071A (en) | 1988-09-17 | 1992-08-11 | Basf Aktiengesellschaft | Process for preparing peptides with n-terminal non-proteinogenous amino acids |
US5157145A (en) | 1988-09-17 | 1992-10-20 | Basf Aktiengesellschaft | Process for the preparation of dipeptides with c-terminal non-proteinogenous amino acids |
US5013795A (en) | 1989-04-10 | 1991-05-07 | Minnesota Mining And Manufacturing Company | Azlactone graft copolymers |
US5185102A (en) | 1989-06-08 | 1993-02-09 | Minnesota Mining And Manufacturing Company | Polymeric charge transfer complexes for nonlinear optical applications |
US4981933A (en) | 1989-06-23 | 1991-01-01 | Polaroid Corporation | Azlactone copolymers |
US5075352A (en) | 1989-08-15 | 1991-12-24 | Minnesota Mining And Manufacturing Company | Stabilized polymeric dispersions |
US5147957A (en) | 1989-09-22 | 1992-09-15 | Minnesota Mining And Manufacturing Company | Hydrosilated azlactone functional silicon containing compounds and derivatives thereof |
US5157108A (en) | 1989-12-12 | 1992-10-20 | Minnesota Mining And Manufacturing Company | Thermally sensitive linkages |
US5066559A (en) | 1990-01-22 | 1991-11-19 | Minnesota Mining And Manufacturing Company | Liquid electrophotographic toner |
US5149806A (en) | 1990-03-28 | 1992-09-22 | Minnesota Mining And Manufacturing Company | Azlactone michael adducts |
US5039813A (en) | 1990-06-29 | 1991-08-13 | Polaroid Corporation | 2-(4-alkenylphenyl)-5-oxazolones and polymers thereof |
US5094766A (en) | 1990-07-02 | 1992-03-10 | Texaco Inc. | Dispersant-antioxidant viscosity index improver |
US5175081A (en) | 1990-08-31 | 1992-12-29 | Minnesota Mining And Manufacturing Company | Post-processsing stabilization of photothermographic emulsions |
US5194623A (en) | 1990-08-31 | 1993-03-16 | Minnesota Mining And Manufacturing Company | Azlactone based photographic reagents |
US5091489A (en) | 1990-10-23 | 1992-02-25 | Minnesota Mining And Manufacturing Company | Oligo (2-alkenyl azlactones) |
US5081197A (en) | 1990-10-23 | 1992-01-14 | Minnesota Mining And Manufacturing Company | Oligo(2-alkenyl azlactones) |
US5200471A (en) | 1990-11-05 | 1993-04-06 | Minnesota Mining And Manufacturing Company | Biomolecules covalently immobilized with a high bound specific biological activity and method of preparing same |
US5981467A (en) * | 1995-03-27 | 1999-11-09 | Arqule, Inc. | Aminimide-containing molecules and materials as molecular recognition agents |
Non-Patent Citations (229)
Title |
---|
"Synthesis of 2,2′-Bis-[5(4H)-oxazolones]" by Charles S. Cleaver et al, 1954, vol. 77, pp. 1544-1546. |
"Synthesis of 2,2'-Bis-[5(4H)-oxazolones]" by Charles S. Cleaver et al, 1954, vol. 77, pp. 1544-1546. |
Acc. Chem. Res. 1981, 14, 356-362, "Alamethicin, a Transmembrane Channel", Ramakrishnan Nagaraj et al. |
Ace. Chem. Res. 1981, 14, pp. 356-362, "Alamethicin, a Transmembrane Channel" by Ramakrishnan Nagaraj et al. |
Acta Chem. Scand. 9 (1955), No. 9, 1498-1509, "The Reaction of Hydrazine with Cinnamic Acid Derivatives", by W.O. Godtfredsen et al. |
Acta Chem. Scand. B 33 (1979) No. 2, "Electron Deficient Heteroar matic Ammonioamidates. XVII. N-(3-Quinazolinio)amindates. VI. The Photochemistry of N-(30Quinazolinio)amidates in the Presence of alpha-Toluenethiol", by G. Barta-Szalai et al. |
Acta Chem. Scand. B 33 (1979) No. 2, "Electron Deficient Heteroar matic Ammonioamidates. XVII. N-(3-Quinazolinio)amindates. VI. The Photochemistry of N-(30Quinazolinio)amidates in the Presence of α-Toluenethiol", by G. Barta-Szalai et al. |
Acta Cryst. (1980), B36, 1498-1500, "Structure of a Peptide Oxazolone: 2-(1′-Benzyloxycarbonylamino-1′-methylethyl)-4,4-dimethyl-5-oxazolone", by C.M.K. Nair et al. |
Acta Cryst. (1983), C39, 894-896, "tert-Butyloxycarbonyl-α-aminoisobutyryl-α-aminoisobutyrate Benzyl Ester, C20H30N2O5", by Patrick Van Roey et al. |
Aminimides, vol. 3, No. 6, Nov.-Dec. 1970, 715-722, "Aminimides. VIII Synthesis and Homo-and Copolymerization Studies of 1,11-Trimethylactrylylhydrazinium Chloride and 1,1,1-Trimethylmethacrylylhydrazinium Chloride", by B.M. Culbertson et al. |
Angew Chem. Int. Ed. Engl. 18 (1979), No. 11, Enantioselective Synthesis of α-Methyl-αaminocarboxylic Acids by Alkylation of the Lactim Ether of cyclo-(I-ala-I-Ala), by Ulrich Schollkopf et al. |
Angew, Chem. Internat. Edit., vol. 14(1975), No. 8, "Applications of Field Desorption Mass Spectrometry in Inorganic Chemistry: Salts", by H.R. Schulten. |
Angew. Chem., 90 (1978), Nr. 2, pp. 136-138, "Asymmetrische Syntheses von x-Alkyl-x-aminocarbon-sauren durch Alkylierung von 1-chiral-substituierten 2-Imidazonin-5-onen", by Von Ulrich Schollkopf et al. |
Angew: Chem. Int. Ed. Engl. 23 420-429, 1984, Pyrylium Mediated Transformations of Primary Amino Groups into Other Functional Groups, by Alan R. Katritzky et al. |
Applied Polymer Symposium No. 26, 399-410 1975, "Synthesis and Polymerization Studies of Aminimide Monomers Containing Acetoxyl or Carboxylic Acid Residues", by B.M. Culbertson et al. |
B.M. Culbertson, R.E. Frais, and D. Grate, Polymer Science: Part A-1, No. 12, vol. 9, 3453-3470, 1971. |
Biochemical and Biophysical Research Communications, vol. 103, No. 3, 1981, pp. 898-904, "Hydrophobic Channels in Crystals of an x-Aminoisobutyric Acid Pentapeptide", by Ch. Pulla Rao et al. |
Biochemical and Biophysical Research Communications, vol. 79, No. 1, 1977, "The Crystal and Molecular Structure Of The Amino Terminal Tetrapeptide of Alamethicin. A Novel 310 Helical Conformation", by N. Shamala et al. |
Biochemical and Biophysical Research Communications, vol. 79, No. 1, 1977, The Crystal and Molecular Structure of the Amino Terminal Tetrapeptide of Alamethicin. A Novel 310 Helical Conformation. |
Biophy.J., vol. 64, Apr. 1993, 1017-1028, "The permeation properties of small organic cations in gramicidin A channels", by Sang-Ah Seoh. |
Biopolymers, vol. 12, 2599-2605 (1973), "An Obligatory a-Helical Amino Acid Residue" by Antony W. Burgess et al. |
Biopolymers, vol. 17, 1693-1711 (1978), "Experimental Conformational Study of Two Peptides Containing a-Aminoisobutyric Acid. Crystal Structure of N-Acetyl-a-Aminoisobutyric Acid Methylamide" by A. Aubry et al. |
Biopolymers, vol. 21, 2461-2472 (1982), "Molecular Structure of t-Butyloxycarbonyl-Leu-Aib-Pro-Val-Aib-Methyl Ester, a Fragment of Alamethicin and Suzukacillin: a 310-Helical Pentapeptide", by Ch. Pulla Rao et al. |
Biopolymers, vol. 22, 1499-1505 (1983), "Crystal Structure of Boc-Ala-Aib-Ala-Aib-Aib-Methyl Ester, A Pentapeptide Fragment of the channel-Forming Inonophore Suzukacillin", by A.K. Francis et al. |
Biopolymers, vol. 22, 205-215(1983), Preferred Conformations of Peptides Containing α,α-Disubstituted α-Amino Acids, by Claudio Toniolo et al. |
Biopolymers, vol. 22, 241-246(1983), "Stabilizing Effects of 2-Methylalaline Residues on beta-Turns and alpha-Helixes", by G. Jung. |
Biopolymers, vol. 22, 241-246(1983), "Stabilizing Effects of 2-Methylalaline Residues on β-Turns and α-Helixes", by G. Jung. |
Biopolymers, vol. 22, 517-530(1983), "Conformational and Dynamic Considerations in the Design of Peptide Hormone Analogs", by Victor J. Hruby et al. |
Biopolymers, vol. 32, 407-410 (1992), "Peptidomimetics as Receptors Agonists or Peptidase Inhibitors: A Structural Approach in the Field of Enkephalins, ANP and CCK" by Bernard P. Roques. |
Bull Chem. Soc. Japan, 1980, 53, 1149, "Reaction of Ethyl Aziodoformate with Morpholines", by Teruko Tshuchida et al. |
Bull Chem. Soc. Japan, 1983, 2073, "Double Cycloaddition Reaction of Imidazolium Methylides. Intermolecular 1,3-Dipolar and Intramolecular Diels-Alder Cycloaddition Reactions", by Otohiko Tsuge et al. |
Bull. Soc. Chem., France—1969 No. 6, 2175-2179, "No. 382—Syntheses Photochimique de (1-H)-Diazepines-1,2" by Jacques Streith et al. |
Bull. Soc. Chim. Belg., 65, pp. 291-296, 1956, "Syntheses des isocyanates de vi2nyle et d'isoprpenyle", by R. Hart. |
Bull. Soc. Chim. Belg., vol. 84/n4/1975, pp. 299-304, "Synthesis of a Homologous Series of Protected Oligopeptides Derived From L-Norvaline" by G.M. Bonora et al. |
Can. J. Chem., vol. 52, 1974, 3671-3675, "New Route to Cyclic Azomethine Imines", By P.C. Ip et al. |
Canadian Journal of Chemistry, vol. 45, 1967, 2619-2622, "Aminimides. II. A one-step synthesis of aminimides from carboxylic acid esters", by William J. McKillip. |
Canadian Journal of Chemistry, vol. 45, 1967, Aminimides. I. "A General Synthesis of Aminimides From Acyl Hydrazides and Their Pyrolysis", by William J. McKillip. |
Canadian Journal of Chemistry, vol. 45, 2625, (1967), "Aminimides. III. A convenient synthesis of isopropenyl isocyanate", by Robert C. Slagel et al. |
Canadian Journal of Chemistry, vol. 50, 1972, "Reaction of Diphenylcyclopropenethione with Pyridinium Imines", by J.W. Lown et al. |
Chem Pharm Bull, vol. 11 (1963), pp 774-748, "Pyridazine Derivatives IV. The Structures of Aminopyridazines", by Yoshiro Nitta. |
Chem. Ber. III, 780-790 (1978), "Pyrazolium-Betaine aus 1, 1-Dialkylhydrazinen und Acetylencarbonsaureestern", by Wolfgang Sucrow et al. |
Chem. Berg. 103, 2052-2061 (1970), Umlagerung von quartaren Allyl-, Benzyl- und Propargyl-hydraziniumsalzen, by Karl-Heinz Konig et al. |
Chem. Phar. Bull., vol. 23, 1975, 452-455, "Studies on Ketene and Its Derivatives. LXVIII Reaction of Kiketene with N-Imino-pyridinium, -quinolinium, and -isoquinolium Ylides", Tetsuzo Kato et al. |
Chem. Pharm. Bull. 31(12)4568-4572 1983, "Thermal Rearrangements of Cyclic Amine Ylides. III.1) Intramolecular Cyclization of 2-Ethynylpyridine N-Imides to 3-Azaindolizine Derivatives", by Takashi Tsuchiya et al. |
Chem. Pharm. Bull. 39 (3) 786-791 1991, "Synthesis and Anti-inflammatory Activities of Some N-[Pyridyl(penyl)carbonylamino]-tert-butyl/phenyl-1,2,3,6-tetrahydropyridines" by Kinke K. Redda et al. |
Chem. Pharm. Bull., 30 (10)3757, 1982, "Studies on Diazepines. XVIII. Photochemical Synthesis of 3H-1,3-Benzodiazepines from Quinoline N-Acylimides", by Takashi Tsuchiya et al. |
Chem. Pharm. Bull., vol. 14(5) 518-523, 1966, "Reaction of N-Aminopyridinium Derivatives.V. Syntheses of 1-(N-Methylacetamido)alkylpyridinium Salts and Their Reaction with Cyanide Ion", by Toshihiko Okamoto et al. |
Chem. Pharm. Bull., vol. 31, 1983, 1378-1381, "1,3-dipolar Cycloaddition Reaction of 1-Methylperimidine 3-Ylides with Dimethyl Accetylenedierboxylate", by Yasumitsu Tamura et al. |
Chem. Pharm.Bull., 19(6)1285-1286 1971, "The Photo Arrangement and Thermolysis of N-Benzoylimino-isoquinolinium and Quinolinium Betaines", by Yasumitsu Tamura et al. |
Chemica Scripta. 1978-79, 13, 195-196, "Electron Deficient Heteroaromatic Ammonioamidates, 201; N-(3-Quinazolinio)amidates, 81", by M. Lempert-Sreter, et al. |
Chemical Abstracts, vol. 114, 1991, p. 40, "Antiarrhythmic effect of adaptive activation of the vagal system and a new synthetic acetylcholine analog", by F.Z. Meerson. |
Chemical Abstracts, vol. 115, 1991, p. 44, "Elimination of disturbances of the heart electric stability and arrhythmias with a synthetic analog of acetylcholine" by F.Meerson et al. |
Chemical Abstracts, vol. 115, 1991, p. 45, "Regulation of the carnitive-dependent metabolism of fatty acids in the rat myocardium", Zh. Shutenko et al. |
Chemical Abstracts, vol. 70, 1969, 264, "Synthesis of 1-alkyl-1,1-dimethylhydrazinium salts and N-alkyldimethylaminoacetimides and their properties", Kameyama, Eiichi et al. |
Chemical Abstracts, vol. 72, 1970, 45292-45293, "Reactive surfactants. II. Synthesis of 2-acyl-1,1,1-trimethylhydrazinium hydroxide inner salts and their properties", by E. Kameyama et al. |
Chemical Abstracts, vol. 89, 1978, p. 250, Mosquito larvicidal and pupicidal activity of aminimides, by E. Clarke et al. |
Chemical Communications, 1965, 120, "The Pyrolysis and Photolysis of Trimethylamine Benzimide", by Richard F. Smith. |
Chemical Communications, 1968, 917-918, "The Crystal Structure of a Novel Heterocycle containing an Intramolecular Carbon-Nitrogen Hydrogen Bond", by Charles J. Fritchie et al. |
Chemical Communications, No. 14, Jul. 21, 1971, 725-726, "Crystal and Molecular Structures of Two N-Ammonio-amidates", by A.F. Cameron. |
Chemical Reviews, 1973, vol. 73, No. 3, pp. 255-281, "The Chemistry of Aminimides", by W.J. McKillip et al. |
Chemistry and Industry, Jul. 11, 1970, "Kinetics of reaction between gaseous oxygen and cobalt(II) ammines" by R. Bratchley et al. |
Chemistry Department of the University of Michigan, Sep. 1959, 1325-1332, vol. 24, "Nitroative Cleavage of N′,N′-Dialkylhydrazides and Tertiary Amines", by Peter Smith et al. |
Chemistry Letters, pp. 413-414, 1976, "Synthesis and Characterization of 1-Imidoyliminopyridinium N-Ylides", by Akikazu Kakehi et al. |
Communications, Dec. 1981, pp. 969-971, Asymmetric Syntheses via Heterocyclic Intermediates; VIII. Enantioselective Synthesis of (R)-α-Methyl-α-amino Acids using L-Valine as Chiral Auxiliary Reagent by Ulrich Schollkopf et al. |
Coyright 1981 by Walter de Gruyter Berlin, Structure and Activity of Natural Peptides, Properties of the Membrane Modifying Polypeptide Antibiotics Alamethicin and Trichotoxin A-40, by Gunther Jung. |
Die Angewandte Makromolekulare Chemie 11 (1970) 109-124, "Syntheses und Reaktionen von 2-Alkenyloxazolonen" by Von Klaus Hubner et al. |
Eur. J. Med. Chem.—Chem. Ther. 1982-17, N. 3, pp 265-270, "Aminimides ethyleniques a action vasodilatatrice peripherique", by Mohamed Tichniouin et al. |
Gaza Chem. Ital. 95, 1965, "Reazione dei diarildiazoalcani-Nota IV. Difenildiazometano e azoici carbonilici", Gian Franco Bettinetti et al. |
Gazzetta Chimica Italiana, 117, 1987, 509-511, "The Structure of the Pyridine 1-Benzimide Mono Cation", by Alan R. Katritzky. |
Helvetica Chimica Acta—vol. 65, Fasc. 1 (1982)-Nr. 18, "18. Azimine. V. 12) 1-Alkoxycarbonyl-2,3-dialkyl- und -2,3-diaryl-azimine" by von Christian Leuenberger. |
Heterocycles, vol. 18, 1982, "Pyrazolo(1,5-c)Pyrimidines from pyrylium Salts and Amidrazones and Pyridine Imidoyl-N-Imides from Imidoyl Chlorides", by Alan R. Katritzky et al. |
Inorg. Nucl. Chem. Letters, vol. 10, pp 233-235, 1974, "Ortho-Metallation Reactons With 1-Benzoyliminopyridinium Betaine", by Shelton A. Dias et al. |
Int. J. Peptide Protein Res. 19, 1982, 499-505, "Crystal and molecular structure of tert.-butyloxycarbonyl-L-hydroxy-prolyl-α-aminoisobutyryl-α-aminoisobutryl-L-phenylalaninol" by Parick Van Roey et al. |
Int. J. Peptide Protein Res. 21, 1983, 392-405, "Peptides containing dipropylglycine", by Paul M. Hardy et al. |
Int. J. Peptide Protein Res. 22, 1983, 603-610, "Bioorganic stereochemistry", by Claudio Toniolo et al. |
Intra-Science Chemistry Reports, vol. 5, No. 4, 1971, pp. 305-316 "Studies on the Biologically-Active Conformations of Angiotensin" by Garland. |
I-Pharmacology, vol. 108, 1988, pp 31589, "Regulation of carnitive-dependent metabolism of fatty acids in myocardium under the influence of 3-(2,2,2-tri-methylhydrazinium)propionate" Zh. Shutenko et al. |
J. Am. Chem. Cos., 1981, vol. 103, pp. 1493-1501, "Crystal Structures and Conformational Calculations of Fragments of Alamethicin Containing Aminoisobutyric" by G. David Smith. |
J. Am. Chem. So., 1982, 104, pp. 2437-2444, Solid-State and Solution Conformation of Homo Oligo (alpha-aminoisobutyric aids) from Tripeptide to Pentapeptide: Evidence for a 310 Helix1a . |
J. Am. Chem. So., 1982, 104, pp. 2437-2444, Solid-State and Solution Conformation of Homo Oligo (α-aminoisobutyric aids) from Tripeptide to Pentapeptide: Evidence for a 310 Helix1a . |
J. Am. Chem. Soc. 1984, 106, 8146-8152, Folded and Extended Structures of Homooligopeptides from alpha,alpha-Dialkylated Glycines. A Conformational Energy Computation and X-ray Diffraction Study, Ettore Benedetti et al. |
J. Am. Chem. Soc. 1984, 106, 8146-8152, Folded and Extended Structures of Homooligopeptides from α,α-Dialkylated Glycines. A Conformational Energy Computation and X-ray Diffraction Study, Ettore Benedetti et al. |
J. Am. Chem. Soc. 1984, 106, 8152-8156, "Folded and Extended Structures of Homooligopeptides from alpha,alpha-Dialkylated alpha-Amino Acids. An Infrared Absorption and H Nuclear Magnetic Resonance Study", by Gian Maria Bonora. |
J. Am. Chem. Soc. 1984, 106, 8152-8156, "Folded and Extended Structures of Homooligopeptides from α,α-Dialkylated α-Amino Acids. An Infrared Absorption and H Nuclear Magnetic Resonance Study", by Gian Maria Bonora. |
J. Am. Chem. Soc. 1991, 113, 2275-2283, "Topographic Design of Peptide Neurotransmitters and Hormones on Stable Backbone Templates: Relation of conformation and Dynamics to Bioactivity" by Wieslaw M. Kazmierski et al. |
J. Am. Chem. soc., 1982, 104, 2437-2444, "Solid-State and Solution Conformation of Homo Oligo-alpha-aminoisobutyric acids) from Tripeptide to Pentapeptide: Evidence for a 310 Helix1a", by Ettore Benedetti. |
J. Am. Chem. soc., 1982, 104, 2437-2444, "Solid-State and Solution Conformation of Homo Oligo-α-aminoisobutyric acids) from Tripeptide to Pentapeptide: Evidence for a 310 Helix1a", by Ettore Benedetti. |
J. Am. Chem. Soc., vol. 103, No. 11, 1981, pp. 2948-2955, "Sensitivity of Polypeptide Conformation to Geometry. Theoretical Conformational Analysis of Oligomers of -Aminoisobutyric Acid", by Yvonne Paterson et al. |
J. Chem Soc., 162, 1975, J.C.S. Dalton, "Metal-Ylide Complexes. Part I. Metallation Reactions . . . ", by Shelton A. Dias et al. |
J. Chem Soc., 1972, 1071-1076, "Structural Investigations of Ylides. Part I. Crystal and Molecular Structures of Trimethylammoniobenzamidate and Trimethylammonionitramidate: Two Stabilised Nitrogen-Nitrogen Ylides", by A.F. Cameron. |
J. Chem. Research (S), 192-193, 1988, "Photochemistry of Trialkylammonio-N-benzoylimides: Rearrangement and Amide Formation" by Sally Freeman et al. |
J. Chem. Research(S), 354-355 1989, "Base-induced Rearrangement of 1,1,1,2-Tetrethyl-2-benzoylhydrazinium Iodide to N-(Dimethylaminomethyl)-N-methylbenzamide" by Sally Freeman et al. |
J. Chem. Soc. (C), 1967, 2577-2580, Thermolysis of Trimethylamine-benzimide and Related Compounds: Identification of By-products and their Probable Mechanism of Formation by Martin S. Gibson et al. |
J. Chem. Soc. Perkin Trans. 1 1983, "Electron Deficient Heteroaromatic Ammonioamides., etc.", by Magda Lempert-Sreter et al. |
J. Chem. Soc. Perkin Trans. 11, 1993, "On the Nature of Nitrogen—Nitrogen Bonding in Cyclic Aminimides", Shinji Tsuchiya. |
J. Chem. Soc. Perkin Trans. 1988, "Reactions of Some 1,3-Diaminonucleophiles with Azlactones" by Ahmad M. Tikdari et al. |
J. Chem. Soc. Perkin Trans. II 1982, pp. 1235-1239, "The Crystal Structure of the Amino-terminal Pentapeptide of Suzukacillin. Occurrence of a Four-fold Peptide Helix", by Athappilly K. Francis. |
J. Chem. Soc., Chem Commun., 1982, 875-876, "Evidence for Amide Resonance observed in Cyclic N-Ammonio-imitates by X-Ray Photoelectron Spectroscopy", by Shinji Tsuchiya. |
J. Chem. Soc., Perkin Trans. 1 1983, 417-421, "Molecular Structure of Boc-Aib-Aib-Phe-Met-NH2 DMSO, A Fragment of a Biologically Active Enkephalin Analogue", by B.V. Venkataram Prasad, et al. |
J. Chem. Socl. Perkin Trans. I 1983, "Electron Deficient Heteroaromatic Ammonioamides. Part 24.1. N-(Quinazolin-3-io)amindates. Part 11.2 The Photochemistry of N-(6,7-Methylenedioxyquinazolin-3-io)amidates in Acetone", by Gizella Barta-Szalai et al. |
J. Hetegel Chem., 1972, 9, 687-690, "Aminimides IX(1). A general Synthesis of 1-Substituted-2-imidazolidinones(2)", by David Aelony et al. |
J. Heterocyclic Chem., 23, 375, 1986, "Novel Synthesis of Pyridol[2,1-fl]-as-Triazinium System and its Zwitterionic Derivatives . . . ", by S. Batori. |
J. Heterocyclic Chem., 25, 437 (1988), "Regioselectivity in Methylation and Phenylation of the Zwitterionic Pyrido[2, 1-f]-as-triazinium-1- and 3-olates and thiolates[1]", by Sandor Batori et al. |
J. Heterocyclic Chem., 26, (Sep.-Oct. 1989), 1373-1382, Study of the Structure of Besulpamide, 1-[-Chloro-3-sulfamoylbenzoyl)amino]2,4,6-trimethylpyridinium hydroxide inner salt, and related compounds, using X-ray Crystallography and H and 13C Nuclear Magnetic Resonance Spectroscopy, Jordi Frigola et al. |
J. Heterocyclic Chem., 27, 1041 (1990), "Synthesis of Some N-[Pyridyl(phenyl)carbonylamino]-alkyl-1,2,3,6-tetrahydropyridines", by Kinfe K. Redda. |
J. Heterocyclic Chem., 27, 1673 (1990), "Synthesis and Regiospecificity in Methylation of Pyrido[1,2-a]pyrazinium-1- and 3-olates and Pyrido[1,2-b]pyridazinium-2- and 4-olates [1]", by S. Batori et al. |
J. Heterocyclic Chem., 9, Aug. 1972, 865, "Synthesis of 3-substituted N-Aminopyridinium Salts(I)", by Yasumitsu Tamura et al. |
J. Med. Chem, 1987, 30, 104-108, "Synthesis of N-(3,6-Dihydro-1 (2H)-pyridinyl)benzamides with Hyperglycemic-Hypoglcemic Activity", by Jupita M. Yeung et al. |
J. Med. Chem. 1982, 25, 191-195, "Synthesis of N-(Carbonylamino)-1,2,3,6-tetrahydropyridines with Analgesic, Antiinflammatory, and Hyperglycemic Activity", by Jupita M. Yeung et al. |
J. Med. Chem. 1991, 34, 1777-1789, "Synthesis, Conformational Properties, and Antibody Recognition of Peptides Containing beta-Turn Mimetics Based on a alpha-Alkylproline Derivatives" by Mark G. Hinds. |
J. Med. Chem. 1991, 34, 1777-1789, "Synthesis, Conformational Properties, and Antibody Recognition of Peptides Containing β-Turn Mimetics Based on a α-Alkylproline Derivatives" by Mark G. Hinds. |
J. Med. Chem., 1979, vol. 22, No. 9, 1079, "Syntheses of N-Substituted 2(3,4)-Pyridylcarboxylic Acid Hydrazides with Analgesic and Antiinflammatory Activity", by Knife Redda et al. |
J. Med. Chem., 1982, 25, 720-723, "Synthesis of N-[[(Substituted-phenyl)carbonyl]amino]-1,2,3,6-tetrahydropyridines with Analgesic and Hyperglycemic Activity", by Jupita M. Yeung. |
J. Org. Chem USSR, 1977, 13, 885, "Reaction of Acyl Nitrenes with Unsaturated Compounds", by V.P. Semenov et al. |
J. Org. Chem, USSR 1966, 2, Aminimides cyclic. |
J. Org. Chem., 1981, 46, 2490-2497, Relative Reactivity and Structures of Benzoyltrimethylhydrazine and 1-Benzoyl-2-methylpyrazolidine, by Spencer Knapp. |
J. Org. Chem., 1982, 47, 5023-5025, Degradation of Aminimides Obtained from Enamines and (Ehoxycarbonyl)nitrene, by Lucio Pellacani et al. |
J. Org. Chem., 24, 1825, vol. 28 (1959), "Alkyl-(alkoxyalkyl-)hydrazones", by John C. Howard et al. |
J. Org. Chem., vol. 41, No. 4, 1976, 715-716, "Acyl Migration in 2-Hydroxylalkyl Aminimides", by Meir Asscher. |
J. Org. Chem., vol. 41, No. 9, 1976, 1555-1556, "Reaction of 1,1-Dibenzoyl-2,2-dimethylhydrazine with Methyl p-Toluenesulfonate", by Richard F. Smith. |
J. Org. Chem., vol. 44, No. 16, 1979, 2850-2855, "On the Bond Character of N-Containing Ylides", by Shinji Tsuchiya et al. |
J. Org. Chem., vol. 59, No. 14, 1974, "Sevens Rearrangement of Carbamoylaminimides" by Richard F. Smith et al. |
J. Prakt. Chem. [2] 110, 204, 1925, "Polyspirocyclische Komplexe des Palladiums mit Phosphor-Yliden", by Hubert Schmidbaur et al. |
J.C.S. Chem. Comm., 1975, 93-94, "Methylation and Protonation Sites in Some N-Ammonioamidates" by Milica Liler et al. |
J.C.S. Chem. Comm., 1978, pp. 996-997, "The 310 Helical Conformation of a Pentapeptide Containing a-Aminoisobutyric Acid (Aib): X-Ray Crystal Structure of Tos-(Aib)5-OMe", N. Shamala et al. |
J.C.S. Chem.Comm., 1978, 996-997, "The 310 Helical Conformation of a Pentapeptide Containing α-Aminoisobutyric Acid (Aib): X-Ray Crystal Structure of Tos-(Aib)5-OMe" by Narayanaswamy Shamala et al. |
J.C.S. Dalton I, 1978, 1155, "Reactions of 2-Azidopyridine and 1-Pyridinio Ylides with Transition-metal Complexes", by Maddalena Pizzotti. |
J.C.S. Perkin I, 1973, 2580-2583, "Synthesis and Thermal Reaction of 2,2-Diacyl-N-(1-pyridinio)vinyl-aminides: Formation of Pyrazolol[1,5-a]pyridines and Isoxazoles", by Yasumitsu Tamura et al. |
J.C.S. Perkin I, 1979, "Heterocycles in Organic Synthesis. Part 16, The Conversion of Aliphatic, Aromatic, and Heteroaromatic Primary Amines into Iodides" by Alan R. Katritzky et al. |
J.C.S. Perkin I, 1979, "Heterocycles in Organic Synthesis. Part 17, Conversion of Primary Amines into Bromides and Chlorides", by Alan R. Katritzky et al. |
J.C.S. Perkin I, 1979, "Heterocycles in Organic Synthesis. Part 19, Thermolysis of Pyridinium N-Acylimines: a New Preparation of Isocyanates", by Alan R. Katritzky et al. |
J.C.S. Perkin I, 1979, "Heterocycles in Organic Synthesis. Part 19. Thermolysis of Pyridinium N-Acylimines: a New Preparation of Isocyanates", by Alan R. Katritzky et al. |
J.C.S. Perkin I, 1979, "Heterocycles in Organic Synthesis. Part 24. A New Synthesis of NN′-Diarylcarbodi-imides", by Alan R. Katritzky et al. |
J.C.S. Perkin I, 1979, "Heterocycles in Organic Synthesis. Part 24. A New Synthesis of NN'-Diarylcarbodi-imides", by Alan R. Katritzky et al. |
J.C.S. Perkin I, 1981, 1495-1500, "Reactions of Pyryliums with Mono-and asym-Di-substituted Hydrazines" by Alan R. Katritzky et al. |
J.C.S. Perkin II, 1976, "The Basicities of N-Trimethylammonioacetamidate and of Substituted N-Trimethylammoniobenzamidates. The Hammett Correlation and the Thermodynamics of Protonation", by William H. Beck et al. |
J.C.S. Perkin II, 1978, 1173, "The Basicities of Substituted N-Trimethylammoniophenylacetamidates and N-Trimethylammoniocinnamamidates. The Hammett Correlations and the Thermodynamics of Protonation", by William H. Beck. |
J.C.S. Perkin, Trans 2, 1977, 909-914, "Mono- and Di-protonation Sites in N-Ammonio-amidates: a Specro-scopic Study", by Milica Liler. |
J.C.S. Perkins II, 1978, 431, "Basicity of the Carbonyl Group. Part 6, Calorimetric and Spectometric Study of Complexation of para-substituted N-Ammoniobenz-amidates by Boron Trifluoride", by Jean-Francois Gal et al. |
J.C.S. Perkins II, 1980, 380, "The Kinetics of Hydrolysis of N-Trimethylammonioacetamide and of Substituted N-Trimethylammoniobenzamides in Concentrated Sulphuric Acid", by Milica Liler et al. |
J.Org.Chem., Sep. 1965, 3031-3033, "The Rearrangement of 1-Methyl-1-acetylimide-2-phenylpyrrolidine", by S. Wawzonek et al. |
Journal American Chemical Society, vol. 82, 1960, 5718-5721, "The Rearrangement of 1,1-Dimethyl-1-p-nitrobenzylamine-2-acetamide", by S. Wawzonek. |
Journal of Applied Polymer Science, vol. 27, 2361-2368 (1982), "Aminimide as Hardener/Cruing Promotor for One Part Epoxy Resin Composition", by Hideri Nhno and Saburo Noguchi. |
Journal of Applied Polymer Science, vol. 27, 2361-2368 1982, "Aminimide as Hardener/Curing Promoter for One Part Epoxy Resin Composition", by Hideki Niino et al. |
Journal of Chemistry, 1966, vol. 31, 1704-1707, "Cyclic Aminimides", by William S. Wadsworth, Jr. |
Journal of Chemistry, 28, 1963, vol. 28, 2376-2377, The Resolution of 1-Ethyl-methyl-1-p-nitrobenzylamine-2-acetamide, by S. Wawzonek et al. |
Journal of Chemistry, 31, Nov. 1966, 3851-3852, "A Novel Synthesis of 1,5-Diphenylpyrazolone-3", by Henry W. Schiessl et al. |
Journal of Fluorine Chemistry, 51, 1991 419-431, "Amine(polyfluoroalkoxyacyl)imide Surfactants[1]", by Lisa Haywood et al. |
Journal of Molecular Structure, 243 (1991) 365-368, "A Multinuclear NMR Study On Some Cyclic Aminimides and Related Compounds", by J. Jazwinski. |
Journal of Molecular Structure, 86 (1982) 341-347, "Quantum Theory of the Structure and Bonding in Proteins", by David Peters and Jane Peters. |
Journal of Pharmaceutical Sciences, vol. 75, No. 4, Apr. 1986, 407-409, "2,240 -Phthaloyl-, 2,2′-Isophthaloyl-, and 2,2′-Terephthaloylbis[1,1,1-trimethylhydrazinium] Dihydroxie, Bis(Inner Salts): Synthesis, Partition Coefficients, Toxicity and Effect on Ganglionic Transmission", by Lindley A. Cates. |
Journal of Pharmaceutical Sciences, vol. 75, No. 4, Apr. 1986, 407-409, "2,240 -Phthaloyl-, 2,2'-Isophthaloyl-, and 2,2'-Terephthaloylbis[1,1,1-trimethylhydrazinium] Dihydroxie, Bis(Inner Salts): Synthesis, Partition Coefficients, Toxicity and Effect on Ganglionic Transmission", by Lindley A. Cates. |
Journal of Pharmaceutical Sciences, vol. 81, No. 5, May 1992, "Synthesis and Pharmacological Evaluation of Some N-[Pyridyl(phenyl)carbonylamino]methyl-1,2,3,6-tetrahydropyridines" by Kinfe K. Redda et al. |
Journal of Polymer Science, Part A:, Polymer Chemistry, vol. 26, 1779-1789 (1988), "Tough Epoxy Resins Cured with Aminimides", by Shinzo Inubushi et al. |
Journal of Polymer Science, Part A-1, vol. 6, 363-373 (1968), "Aminimides. IV. Homo- and Copolymerization Studies on Trimethylamine Methacrylimide", by B.M. Culbertson. |
Journal of Polymer Science, vol. 22, 3149-3160(1984), "Chemistry of Alkenyl Azlactones. IV. Preparation and Properties of Telechelic Acrylamides Derived from Amine-terminated Oligomers" by Steven M. Heilmann et al. |
Journal of Polymer Science: Part A: Polymer Chemistry, vol. 25, 1363-1382 1987, "Thermal Decomposition Behavior of Bis-aminimides and Their Application to Polymerization of Epoxide" by Shinzo Inubushi et al. |
Journal of Polymer Science: Part A: Polymer Chemistry, vol. 25, 137-150 (1987), "Thermal Decomposition Behavior of Mono-aminimides and Their Application to Polymerization of Epoxide", by Shinzo Inubushi et al. |
Journal of Polymer Science: Part A: Polymer Chemistry, vol. 29, 29-37(1991), "Copolymers of 2-Vinyl-4,4-Dimethylazlactone with Styrene and Ethyl α-Hydroxymethylacrylate" by Jeno Muthiah et al. |
Journal of Polymer Science: Part A-1, vol. 6, 2197-2207 (1968), "Aminimides V. Preparation and Polymerization Studies of Trimethylamine-4-Vinylbenzimide", by B.M. Culbertson et al. |
Journal of Polymer Science: Part C: Polymer Letters, vol. 24, 287-289 (1986), A Polymer whose Aqueous Solutions Show the Properties of Negative Thixotropy and Thermoreversible Gelation: (Poly-Trimethylamine p-Vinylbenzimide), by LLoyd D. Taylor et al. |
Journal of Polymer Science: Polymer Chemistry Edition, vol. 21, 3597-3600 1983, "Synthesis of Polymers Containing Pyridinium Ylide and Iminopyridinium Ylide Structure", by S. Kondo et al. |
Journal of Polymer Science: Polymer Chemistry Edition, vol. 21: 1159-1164 1983, Synthesis of Aminimide Monomers and Polymers, Avinash C. Mehta et al. |
Journal of the American Chemical Society, 101:1, Jan. 3, 1979, "Stereochemically Constrained Linear Peptides. Conformations of Peptides Containing α-Aminoisobutyric Acid", by R. Nagaraj et al. |
Journal of the American Chemical Society, 90:19, Sep. 11, 1968, "Novel Heterocyclic Syntheses from Azomethine Imides. 2-Unsubstituted Diazetidinones", by Ken'ichi Takeuchi, et al. |
Journal of the American Oil Chemists' Society, 52, 1975, "Aminimides: II. Antimicrobial Effect of Short Chain Fatty Acid Derivatives", by J.J. Kabara et al. |
Journal of the American Oil Chemists' Society, vol. 53, 1976, "Synthesis of 1,1,1-Tris(2-hydroxyethyl)amine-2-acylimide", Isao Ikeda et al. |
Journal of the American Oil Chemists' Society, vol. 55, Feb. 1978, "Properties of 2-Hydroxyethylamine Acylimide Aqueous Solution-Unusual Clouding Phenomenon", Isao Ikeda et al. |
Kardiologisisa, "Bioelectrical Mechanism", vol. 31, No. 7, 1991, pp. 52-55. |
Kardiologisisa, vol. 30, No. 8, 1990, pp. 69-72. |
Liebigs Ann. Chem. 1977, 506-527, "Additionen mit Chinolinium-, Isochinolinium- und Phenanthridinium-N-imid", by Rolf Huisgen et al. |
Liebigs Ann. Chem. 1980 715-724, "Die Kristallstruktur von α(tert-Butyloxycarbonylamino)-isobuttersaure" by Wilfried Mayr et al. |
Liebigs Ann. Chem. 1982, 1304-1321, "The α-Helical Conformation of the Undecapeptide Boc-L-Ala-[Aib-Ala]2-Glu(OBzl)-Ala-[Aib-Ala]2-OMe: Synthesis, X-ray Crystal Structure, and Conformation in Solution", by Heribert Schmitt. |
Liebigs Ann. chem. 1988, 1025-1031, "Asymmetric Synthesis of Boc-L-Val-(R)-α-MePro-OMe, Boc-L-Val-(R)-Proome, and of Boc-L-Val-(R)-α-MePhe-OMe, Ac-L-Val-(R)-α-MePhe-OMe and Their Analogues. A New Strategy for the Synthesis of Non-Proteinogenic Dipeptides", by Ulrich Schollkopf. |
Lipids, vol. 20, No. 10 (1985), 685-692, "Hypolipidemic Activity of the Surfactants Aminimides, and Their Effects on Lipid Metabolism of Rodents", by Iris H. Hall. |
M.R.Chemistry, vol. 20, 1988, 471-474, "Synthesis and Spectroscopic Studies of 2-(1,1-Dimethylhydrazono)propyl Phosphonates" by Miguel Salazar et al. |
Macromolecules, vol. 1, p. 254, May-Jun. 1968, "Aminimides. VII. Homo- and Copolymerization Studies on 1,1-Dimethyl-1-(2-hydroxypropyl)amine-Methyacrylimide . . . ", by B.M. Culbertson. |
Makromol Chem., Rapid Commun. 3, 779-782(1982), "Synthesis of Poly(4,4-dimethyl-2-vinyl-5-oxazolone) an Interesting Material for Preparing Polymeric Agents", by Lloyd D. Taylor et al. |
Makromol. Chem., Rapid Commun. 5,67-70 (1984), "Chemistry of Alkenylazlactones, 2a) Reaction with thiols", by Jerald K. Rasmussen et al. |
Meth and Find Exptl Clin Pharmacol 1987; 9(2):101-110, "Pharmacological Properties of Besulpamide, a New Diuretic, in Rats and Dogs", by M. Colombo, et al. |
Meth and Find Exptl Clin Pharmacol 1987; 9(2):111-119, "Acute, Subacute and Subchronic Toxicity of Besulpamide", by I. Demestre et al. |
Meth and Find Exptl Clin Pharmacol 1987; 9(2):121-126, "Pharmacokinetics of Besulpamide in Rats and Dogs", by J. Esteve. |
Monatshefte fur Chemie, 120, 749-758 (1989), "1-Amino-2-hydrazinopyrimidin-N-ylides. Unusual Tautomers of 1-Aminopyrimidin-2-hydrazones", by Jurgen Liebscher. |
Nature, vol. 300, Nov. 1982, pp. 325-330, Articles—"A voltage-gated ion channel model inferred from the crystal structure of alamethicin at 1.5-A resolution", by Robert O. Fox, Jr. & Frederic M. Richards. |
Newcastle Technical Centre, 1274-1280, Jun. 1969, "Light Scattering by Polydisperse Cylindrical Micelles", by J.M. Corkill et al. |
Nippon 1974, No. 9, 1789, "Preparation and Some Properties of (2-Hydroxyalkyl)-dimethylammonium-N-acylimine", by Eiichi Kameyama et al. |
Nucleosides & Nucleotides, 10(8), 1657-1665, 1991 "Synthesis of N-Aminopyrazinium Analogs of Cytidine and 2′-Deoxycytidine", by Miroslav Bobek et al. |
Nucleosides & Nucleotides, 10(8), 1657-1665, 1991 "Synthesis of N-Aminopyrazinium Analogs of Cytidine and 2'-Deoxycytidine", by Miroslav Bobek et al. |
Organic Mass Spectrometry, 1971, vol. 5, pp 61 to 71, "The Mass Spectra of N-Acyliminopyridinium and Isoquinolinium Betaines", by M. Ikeda et al. |
Organic Preparations and Procedures 1(3), 217-219 (1969), "A convenient synthesis of 5-oxazolones. 2-phenyl-5-oxazolone" by Lloyd D. Taylor et al. |
Organic Preparations and Procedures 1(3), 217-219(1969), "A convenient Synthesis of 5-oxazolones. 2-Phenyl-5-oxazolone", by L.D. Taylor et al. |
Organic Preparations and Procedures Int. 13(1), 55-58, 1981, "Preparation of 2-Hydroxyethyldimethylamine Acylimides" by Robert J. Small. |
Organic Preparations and Procedures Int. 8(5), 215-217 (1976), "Electrolytic Preparation of bis-Dimethyl-2-Hydroxypropylamineazobenzimides", by S. Wawzonek et al. |
Plastics Manufacturing., vol. 83, 1975, "Amine imides" by Kanji Matsueda et al. |
Polymer Bulletin 22, 449-454(1989), "Synthesis and reactivity of highly versatile VDMO-VBC copolymers" by Robert C. Fazio et al. |
Polymer Letters, vol. 2, pp. 1095-1096 (1964), "Thermally Reversible Homopolymer Gel Systems", by Howard Haas et al. |
Polymer Letters, vol. 7, pp. 597-603(1969), "The Synthesis of Vinyl Peptide Monomers", by L.D. Taylor et al. |
Polymer Letters, vol. 9, pp. 187-190(1971), "Synthesis and Polymerization of 2-vinyl-4,4-Dimethyl-5-Oxazolone" by L.D. Taylor et al. |
Rubber Chem. Technology, 53, 1980, "Halogen-containing Aminimide Compounds as Tire Cord Adhesives", P.E. Throckmorton et al. |
Supplement II to Circulation Research, vol. XXX and XXXI, Sep. 1972, pp 143-150, "Angiotensin II—Studies on the Biologically Active Conformation", by Garland R. Marshall, et al. |
Tetrahedron Letters No. 30, 2621-2624, 1974, "A convenient Thermal Route to N,N-Dialkylaminoisocyanates", by William J.S. Lockley. |
Tetrahedron Letters No. 31, pp 2689-2690, 1976, "Allylic and Benzylic Deamination By Thermal Cleavage of 1-substituted 1,2-Dihydro-2, 4, 6-Triphenylpyridines" by A.J. Boulton et al. |
Tetrahedron Letters No. 31, pp 2691-2694, 1976, "Pyridines as Leaving Groups in Synthetic Transformations: Nucleophilic Displacements of Amino Groups, and Novel Preparations of Nitriles and Isocyanates", by J.B. Bapat et al. |
Tetrahedron Letters No. 37, 3249-3252, 1974, "Cyclic Aminimides Containing the 3-oxo-5-Thioxo-1,2,4-Triazolidine Skeleton: Rearrangements of 5-Thiourazole Derivatives", by V.T. Ramakrishnan. |
Tetrahedron Letters No. 48, 4263-4266, 1974, "Cyclic Aminimides Containing The pyrazolone Skeleton", by William J.S. Lockley. |
Tetrahedron Letters No. 5., 425-428, 1971, "Cycloadditions of Aminoisocyanates to Heterocumulenes", by Walter Lwowski et al. |
Tetrahedron Letters No. 52, pp 4859-4862, 1976, "Regiospecific Versus Non-Regiospecific Photoinduced Ring-Enlargment of 3-Substituted 1-Iminopyridinium Ylides", by Jacques S. et al. |
Tetrahedron Letters vol. 21, 5059-5060, 1980, "New Cyclic Aminimides Containing Pyrazolone Skeleton", By M. Poje and N. Bregant. |
Tetrahedron Letters, 27, 6319 (1986). |
Tetrahedron Letters, No. 26, pp. 1733-1737, 1964, "Beaktionen von Benzol-Derivaten Mit Nitrenen", by Klaus Hafner et al. |
Tetrahedron Letters, No. 4, pp 289-292, 1972, "The Curtius Rearrangement in Aminimides" by Herman P. Benecke et al. |
Tetrahedron Letters, vol. 27, No. 52, pp 6319-1986, "Cyclic Carbalkoxy Aminimides. Synthesis and Thermal Decomposition To Give N, N-Dimethylamino Isocyanate", by Jean-Pierre Senet. |
Tetrahedron Letters, vol. 30, No. 49, pp 6845-6848, 1989, "Asymmetric Synthesis of Unusual Amino Acids: Synthesis of Optically Pure Isomers of α-methyltyrosine", by Ernesto Nicolas. |
Tetrahedron vol. 38, No. 24, pp 3579-3583, 1982, "(-)-Isovaline: Confirmation of its D-(=R)-Configuration by X-Ray Analysis of Its N-Chloroacetyl Derivative", by R. Bosch et al. |
Tetrahedron vol. 38, No. 24, pp 3579-3583, 1982, "(−)-Isovaline: Confirmation of its D-(═R)-Configuration by X-Ray Analysis of Its N-Chloroacetyl Derivative", by R. Bosch et al. |
Tetrahedron vol. 48, No. 23, pp. 4733-4748, 1992, "Asymmetric Synthesis Of Unusual Amino Acids: An Efficient Synthesis of Optically Pure Isomers of beta-Methylphenylalanine" by Ramalinga Dharanipragada et al. |
Tetrahedron vol. 48, No. 23, pp. 4733-4748, 1992, "Asymmetric Synthesis Of Unusual Amino Acids: An Efficient Synthesis of Optically Pure Isomers of β-Methylphenylalanine" by Ramalinga Dharanipragada et al. |
Tetrahedron, 1960, vol. 11, pp. 39 to 51., "Synthesis of Peptides Derived From Alpha-Methylalanine", by M.T. Leplawy et al. |
Tetrahedron, vol. 31, pp2559-2569, 1975, "N-(6,7-Methylenedioxy-3-Quinazolinio)Amidates-I Synthesis Spectra and Some Dark Reactions", J. Fetter. |
Tetrahedron, vol. 38, No. 14, pp. 2165-2181, 1982, "Syntheses von 2-Methylalanin-Peptiden, die pH-Abhangigkeit Ihrer 13C-NMR-Spektren und Eine Neue Methode Zur Auswertung uber CS-Diagramme," by Dieter Leibfritz. |
Tetrahedron, vol. 41, No. 12, 2239-2329, 1985, "Heterocyclic Mesomeric Betaines", by W. David Ollis. |
Tetrahedron, vol. 49, No. 15, pp 3185-3192, 1993, "2-Alkoxycarbonylcycloimmonium Ylides, Efficient 1,4-Dipole Equivalents in the Synthesis of New Conjugated Betaines", by Ana M. Cuadro et al. |
Tetrahedron, vol. 49, No. 18, pp. 3767-3780, 1993, "Electrophilic Amination of Pyrimidine-2-thiones—Synthesis of Zwitterionic 2-Aminothiopyrimidinium-N-ylides, Pyrimidine-2-ones and Bicyclic Pyrimidinium Compounds", byBeate Reimer et al. |
The Chemical Society of Japan, No. 3, 1982, "Synthesis, Surfactant Properties and Catalytic Action of Crown Ethers Bearing Aminimide Group", by Seiichi Inokuma et al. |
The Journal of Organic Chemistry, Aug. 31, 1966, "Synthesis of N-[1-(1-Substituted 2-oxopropyl)]acrylamides and -methacrylamides. Isolation and some Reactions of Intermediates of the Dakin-West Reaction", by Yosmo Iwakura et al. |
The Journal of Organic Chemistry, vol. 33, No. 10, Oct. 1968, "Bridgehead Nitrogen Heterocycles. I. A Convenient Synthesis of Pyrazolo[1,5-a]pyridines", by K.T. Potts et al. |
The Journal of Organic Chemistry, vol. 33, No. 4, Apr. 1968, "Aminimides. VI. Synthesis of Aminimides from Carboxylic Acid Esters, Unsymmetrically Disubstituted Hydrazines, and Epoxides", by R.C. Slagel. |
The Journal of Organic Chemistry, vol. 35, No. 2, Feb. 1970, The Chemistry of Diazepines. The Photochemical Intramolecular 1,3-Dipolar Cycloaddition of Substituted 1-Ethoxycarbonyliminopyridinium Ylides, Tadashi Sasaki, et al. |
University College, Hull, Sep. 27, 1952, pp. 453-456, "The Dehydration and Racemisation of N-Acyl-L-aspartic Acids by Acetic Anhydride", by C.C. Barker. |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050186685A1 (en) * | 2004-01-17 | 2005-08-25 | Gyros Ab | Protecting agent |
US8592219B2 (en) * | 2005-01-17 | 2013-11-26 | Gyros Patent Ab | Protecting agent |
Also Published As
Publication number | Publication date |
---|---|
US5981467A (en) | 1999-11-09 |
US5705585A (en) | 1998-01-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0723441A1 (en) | Aminimide-containing molecules and materials as molecular recognition agents | |
US6271195B1 (en) | Aminimide-containing molecules and materials as molecular recognition agents | |
US4785021A (en) | Adsorbent and method of preparation | |
KR860000526B1 (ko) | 아미노-기능이 부여된 아크릴 공중합체의 제조방법 | |
JPH09507487A (ja) | 選ばれた性質を有するアミンイミドおよびオキサゾロンをベースとした分子の系統的モジュール製造 | |
JP2002080530A (ja) | 固相ペプチド合成のための樹脂 | |
AU689764B2 (en) | Modular design and synthesis of aminimide containing molecules | |
AU678168B2 (en) | Oxazolone derived materials | |
WO1994000509A9 (en) | Oxazolone derived materials | |
US7820785B2 (en) | Solid phase synthesis supports and methods | |
US5670480A (en) | Method of making polymers having specific properties | |
WO1995017903A1 (en) | Modular design and synthesis of oxazolone-derived molecules | |
US5962412A (en) | Method of making polymers having specific properties | |
US20020146684A1 (en) | One dimensional unichemo protection (UCP) in organic synthesis | |
US7034110B2 (en) | Method of identifying chemical compounds having selected properties for a particular application | |
CA2180527A1 (en) | Method of making polymers having specific properties | |
JPH03270731A (ja) | 吸着剤 | |
CA2179984A1 (en) | Modular design and synthesis of oxazolone-derived molecules |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
REMI | Maintenance fee reminder mailed | ||
LAPS | Lapse for failure to pay maintenance fees | ||
STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |
|
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20050807 |